Liquid Ampoule

Product Details:

**Composition:**Amikacin Sulfate Injection is a sterile, aqueous solution containing amikacin sulfate equivalent to 100 mg/2ml of amikacin. The inactive ingredients may include sodium bisulfite, sodium citrate, and water for injection.
**Usage:**Amikacin Sulfate is a broad-spectrum antibiotic primarily used to treat serious bacterial infections. It belongs to the aminoglycoside class of antibiotics and works by inhibiting bacterial protein synthesis. It is effective against various gram-negative bacteria such as Escherichia coli, Klebsiella, Pseudomonas aeruginosa, and certain strains of Staphylococcus aureus.
The usage of Amikacin Sulfate Injection should be strictly according to the prescription and guidance of a qualified healthcare professional. The dosage and duration of treatment depend on the severity of the infection, the patient's age, weight, renal function, and other medical conditions. It is usually administered intravenously or intramuscularly.
**Side Effects:**Although effective, Amikacin Sulfate Injection can cause various side effects, which may include but are not limited to:
1. Nephrotoxicity (kidney damage): Amikacin can be toxic to the kidneys, especially when used in high doses or for prolonged periods. Monitoring of kidney function through regular blood tests is essential during treatment.
2. Ototoxicity (ear damage): Amikacin can cause damage to the inner ear, leading to hearing loss, ringing in the ears (tinnitus), or balance problems (vertigo). These effects may be irreversible.
3. Neurotoxicity: Some patients may experience neurotoxic effects such as dizziness, headache, confusion, or muscle twitching.
4. Allergic reactions: Rarely, patients may develop allergic reactions such as rash, itching, swelling, or difficulty breathing. Severe allergic reactions (anaphylaxis) can occur in rare cases and require immediate medical attention.
5. Superinfection: Prolonged or repeated use of antibiotics like Amikacin can result in the growth of resistant bacteria or fungal infections, leading to superinfection.
6. Injection site reactions: Pain, redness, or swelling at the injection site may occur, especially with intramuscular administration.
7. Gastrointestinal disturbances: Nausea, vomiting, diarrhea, or abdominal pain may occur as side effects of Amikacin therapy.
It's crucial to report any unusual or severe side effects to the healthcare provider promptly. Patients should not adjust the dosage or discontinue the medication without consulting their doctor, as it may lead to treatment failure or worsening of the infection.

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• Production Capacity: 100
• Delivery Time: 6-7 days

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**Composition:**Artemether Injection typically contains 40mg/ml of artemether as the active ingredient. Apart from artemether, the injection may also contain other inactive ingredients necessary for formulation stability and compatibility. These inactive ingredients may include solvents, stabilizers, and preservatives. It's important to check the specific formulation for a comprehensive list of ingredients.
**Usage:**Artemether Injection is primarily used for the treatment of severe malaria caused by Plasmodium falciparum, particularly in cases where oral therapy is not feasible or appropriate. It is typically administered by healthcare professionals in hospital settings. The injection is administered intramuscularly (IM) or intravenously (IV), depending on the severity of the condition and the patient's clinical status.
The dosage and duration of treatment with artemether injection should be determined by a healthcare provider based on factors such as the patient's age, weight, severity of the infection, and other medical conditions. Generally, a loading dose may be administered followed by subsequent doses as directed by the healthcare provider.
It's important to follow the healthcare provider's instructions carefully and complete the full course of treatment even if symptoms improve before the treatment is finished. Failure to complete the full course of treatment may result in the re-emergence of malaria parasites and lead to treatment failure or recurrence of the infection.
**Side Effects:**While artemether injection is generally well-tolerated, like all medications, it may cause side effects in some individuals. Common side effects associated with artemether injection may include:
1. Nausea2. Vomiting3. Abdominal pain4. Dizziness5. Headache6. Fatigue7. Injection site reactions (pain, redness, swelling)8. Muscle pain9. Fever10. Anemia (rare)
Serious side effects such as severe allergic reactions (anaphylaxis) and cardiotoxicity (affecting the heart) are rare but possible. Patients should seek immediate medical attention if they experience symptoms of a severe allergic reaction, such as difficulty breathing, swelling of the face, lips, tongue, or throat, or severe dizziness.
Patients should also inform their healthcare provider of any other side effects or adverse reactions experienced during treatment with artemether injection.
It's important to note that this is not an exhaustive list of side effects, and individuals may experience other side effects not listed here. If any side effects persist or worsen, patients should consult their healthcare provider for further evaluation and management.

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• Production Capacity: 1000
• Delivery Time: 6-7 days

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**Composition:**Each milliliter of ascorbic acid injection contains 250 mg of ascorbic acid (Vitamin C). The injection is typically provided in liquid form in ampoules for intravenous administration.
**Usage:**Ascorbic acid injection is commonly used for various medical purposes, including:
1. **Vitamin C Deficiency:** Ascorbic acid injection is utilized to treat or prevent Vitamin C deficiency, which can occur due to inadequate dietary intake, certain medical conditions, or increased metabolic demands.  2. **Antioxidant Therapy:** Ascorbic acid acts as an antioxidant, helping to neutralize free radicals in the body and protect cells from oxidative stress. It may be used in conditions where antioxidant support is needed, such as during certain illnesses or in individuals with compromised immune systems.
3. **Adjunctive Therapy:** Ascorbic acid injection may be used as adjunctive therapy in certain medical conditions, such as sepsis, burns, or surgical recovery, where there is an increased need for Vitamin C due to tissue repair and immune function.
4. **Iron Absorption:** Vitamin C enhances the absorption of non-heme iron from plant-based foods and iron supplements. Ascorbic acid injection may be administered alongside iron therapy to improve iron absorption in individuals with iron deficiency anemia.
5. **Wound Healing:** Ascorbic acid plays a vital role in collagen synthesis, which is essential for wound healing. It may be used in the management of wounds, burns, or surgical incisions to promote tissue repair.
**Side Effects:**While ascorbic acid injection is generally considered safe when used as directed, it may cause side effects in some individuals. Common side effects may include:
1. **Local Irritation:** Pain, redness, or swelling at the injection site may occur, particularly with intravenous administration.
2. **Gastrointestinal Disturbances:** High doses of ascorbic acid may cause gastrointestinal discomfort, including nausea, vomiting, diarrhea, or abdominal cramps.
3. **Kidney Stones:** Prolonged use of high doses of ascorbic acid may increase the risk of kidney stone formation, especially in individuals with a history of kidney stones or predisposing factors.
4. **Iron Overload:** In individuals with iron overload conditions, such as hemochromatosis, excessive Vitamin C supplementation may exacerbate iron absorption and lead to further complications.
5. **Allergic Reactions:** Rarely, allergic reactions to ascorbic acid injection may occur, presenting as rash, itching, swelling, or difficulty breathing. Immediate medical attention should be sought if any signs of an allergic reaction develop.
6. **Interactions:** Ascorbic acid may interact with certain medications, such as anticoagulants (blood thinners), chemotherapy drugs, or oral contraceptives, affecting their efficacy or increasing the risk of side effects. It is essential to inform healthcare providers about all medications and supplements being taken before starting ascorbic acid injection therapy.
It is important to use ascorbic acid injection under the guidance of a healthcare professional, who can determine the appropriate dosage and monitor for any adverse effects, especially in individuals with underlying medical conditions or concurrent medications.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 6-7 days

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**Composition:**Each liquid ampoule of Betamethasone Sodium Phosphate Injection contains 4 mg of betamethasone sodium phosphate as the active ingredient.
**Usage:**Betamethasone Sodium Phosphate Injection is a corticosteroid medication used to treat various inflammatory conditions, allergic reactions, and autoimmune disorders. It works by reducing inflammation, suppressing the immune system, and relieving symptoms such as swelling, redness, itching, and allergic reactions.
This medication is typically administered by injection into a muscle (intramuscular) or vein (intravenous) by a healthcare professional. The dosage and frequency of administration depend on the condition being treated, the patient's response to treatment, and other factors determined by the healthcare provider.
It is crucial to follow the dosage and administration instructions provided by your healthcare provider and to not exceed the prescribed dose. Abruptly stopping treatment with corticosteroids can lead to withdrawal symptoms and worsening of the underlying condition.
**Side Effects:**While Betamethasone Sodium Phosphate Injection can be effective in treating various conditions, it may also cause side effects. Common side effects may include:
1. Increased appetite2. Weight gain3. Fluid retention4. Elevated blood pressure5. Mood changes, including irritability or agitation6. Insomnia7. Glucose intolerance or diabetes8. Skin reactions, such as acne or thinning of the skin9. Increased susceptibility to infections10. Delayed wound healing
It is essential to report any severe or persistent side effects to your healthcare provider promptly. Long-term or excessive use of corticosteroids may also lead to more serious side effects, including osteoporosis, adrenal suppression, and increased risk of infections.
Additionally, Betamethasone Sodium Phosphate Injection may interact with other medications or medical conditions. Inform your healthcare provider about all the medications you are taking, including prescription, over-the-counter, and herbal supplements, before starting treatment with this medication.
Do not suddenly stop using Betamethasone Sodium Phosphate Injection without consulting your healthcare provider, as it may lead to withdrawal symptoms or a flare-up of the underlying condition. Your healthcare provider will gradually reduce the dosage to safely discontinue treatment when appropriate.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 6-7 days

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**Composition:**Bupivacaine hydrochloride injection contains the active ingredient bupivacaine hydrochloride, which is a local anesthetic belonging to the amide group. Each liquid ampoule typically contains 5mg of bupivacaine hydrochloride along with appropriate excipients.
**Usage:**Bupivacaine hydrochloride injection is primarily used as a local anesthetic for various medical procedures. It works by blocking nerve impulses, thereby numbing the area where it is administered. Some common uses include:
1. **Regional Anesthesia:** Bupivacaine is often used for regional anesthesia, such as epidurals for childbirth, nerve blocks for surgery, or spinal anesthesia for procedures below the waist.  2. **Pain Management:** It can be used for postoperative pain management or for pain relief in chronic conditions when administered by healthcare professionals.
3. **Dental Procedures:** Bupivacaine may be used in dental procedures to numb the area around the teeth and gums.
4. **Minor Surgical Procedures:** It can be used for minor surgical procedures to provide localized anesthesia.
**Side Effects:**While bupivacaine is generally considered safe when used appropriately, like all medications, it can cause side effects in some individuals. Common side effects may include:
1. **Nausea and Vomiting:** Some individuals may experience nausea or vomiting after receiving bupivacaine injections.
2. **Dizziness or Lightheadedness:** Bupivacaine can sometimes cause dizziness or lightheadedness, especially if administered in larger doses or if the patient is sensitive to its effects.
3. **Numbness or Tingling:** Temporary numbness or tingling at the injection site or in other parts of the body may occur.
4. **Headache:** Headaches can occur as a side effect of bupivacaine administration, although they are usually mild and transient.
5. **Hypotension:** Bupivacaine can cause a drop in blood pressure, leading to hypotension, especially if administered rapidly or in high doses.
6. **Allergic Reactions:** In rare cases, individuals may experience allergic reactions to bupivacaine, which can manifest as itching, rash, or difficulty breathing. 
7. **Cardiovascular Effects:** Bupivacaine can have effects on the heart and cardiovascular system, including slowing heart rate or, in rare cases, more serious cardiac effects.
It's essential for healthcare providers to monitor patients closely during and after administration of bupivacaine to watch for any adverse reactions and to manage them appropriately if they occur. Additionally, patients should always inform their healthcare providers of any allergies or medical conditions they have before receiving bupivacaine injections.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 6-7 days

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**Composition:**
Each milliliter of Chlorphenamine Injection contains 10 milligrams of Chlorphenamine Maleate as the active ingredient.
Inactive ingredients may include water for injection, sodium chloride, and/or other excipients for formulation stability.
**Usage:**
Chlorphenamine Injection is typically administered intravenously (IV) or intramuscularly (IM) under the supervision of a healthcare professional. It is commonly used for the management of allergic reactions such as:
1. **Allergic Rhinitis:** For the relief of symptoms associated with allergic rhinitis, including sneezing, itching, runny nose, and nasal congestion.2. **Allergic Conjunctivitis:** To alleviate symptoms of allergic conjunctivitis, such as redness, itching, and watering of the eyes.3. **Urticaria (Hives):** For the treatment of acute episodes of urticaria, characterized by raised, itchy welts on the skin.4. **Allergic Dermatitis:** In the management of allergic skin reactions like eczema or contact dermatitis.5. **Anaphylactic Reactions:** As an adjunctive therapy in the treatment of severe allergic reactions or anaphylaxis, alongside other appropriate measures such as epinephrine and corticosteroids.
The dosage and frequency of Chlorphenamine Injection administration depend on the severity of the allergic condition, the patient's age, weight, and overall health status. It's crucial to follow the instructions provided by the healthcare provider or as indicated on the product label.
**Side Effects:**
While Chlorphenamine Injection can be effective in managing allergic symptoms, it may also cause certain side effects. Common side effects associated with Chlorphenamine administration include:
1. **Drowsiness:** Chlorphenamine is a first-generation antihistamine known to cause sedation in many individuals. This drowsiness may impair cognitive and motor functions, affecting activities such as driving or operating machinery.2. **Dry Mouth:** Anticholinergic effects of Chlorphenamine can lead to reduced saliva production, resulting in a dry sensation in the mouth.3. **Blurred Vision:** Some patients may experience temporary visual disturbances or blurred vision while taking Chlorphenamine.4. **Urinary Retention:** In rare cases, Chlorphenamine may cause difficulty or inability to urinate due to its anticholinergic effects.5. **Gastrointestinal Disturbances:** Nausea, vomiting, or constipation may occur in some individuals.6. **Allergic Reactions:** Although rare, hypersensitivity reactions such as skin rash, itching, or swelling may occur.
It's essential to promptly report any unexpected or severe side effects to a healthcare professional. Additionally, patients should avoid consuming alcohol or other central nervous system depressants while taking Chlorphenamine, as it can enhance sedative effects. Individuals with certain medical conditions such as glaucoma, prostate enlargement, or urinary retention should use Chlorphenamine with caution and under medical supervision.

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• Production Capacity: 1000
• Delivery Time: 6-7 days

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**Composition:**
Each liquid ampoule of Cimetidine Injection 100mg contains:- Cimetidine 100mg (as the active ingredient)- Sodium Chloride (as a diluent)- Water for Injection (as a solvent)
**Usage:**
Cimetidine Injection is a medication primarily used to treat conditions such as peptic ulcers, gastroesophageal reflux disease (GERD), and other related gastrointestinal disorders. It belongs to a class of drugs known as H2 receptor antagonists, which work by reducing the production of stomach acid.
The injection form is usually administered in a hospital or clinical setting under the supervision of a healthcare professional. The dosage and frequency of administration will be determined by the treating physician based on the patient's condition and response to treatment.
It is important to follow the instructions provided by the healthcare provider regarding the dosage and administration of Cimetidine Injection. Do not self-administer this medication or change the dosage without consulting a healthcare professional.
**Side Effects:**
While Cimetidine Injection is generally well-tolerated, it may cause certain side effects in some individuals. Common side effects may include:- Headache- Dizziness- Nausea- Diarrhea- Constipation- Fatigue- Muscle pain- Rash or itching
In rare cases, more serious side effects may occur, such as:- Allergic reactions (e.g., rash, itching, swelling of the face, lips, or tongue, difficulty breathing)- Confusion- Hallucinations- Depression- Irregular heartbeat- Liver problems (e.g., jaundice)
If any of these side effects occur or persist, it is important to inform a healthcare professional promptly. Additionally, seek immediate medical attention if you experience any severe allergic reactions or symptoms of a serious condition.
This list of side effects is not exhaustive, and other side effects may occur. It is essential to discuss any concerns or potential side effects with a healthcare provider before starting treatment with Cimetidine Injection.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 6-7 days

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**Composition:**Cyanocobalamin Injection contains cyanocobalamin as the active ingredient. Each milliliter (ml) of the injection typically contains 1 milligram (mg) of cyanocobalamin. Cyanocobalamin is a synthetic form of vitamin B12, which plays a crucial role in various bodily functions, including red blood cell formation, neurological function, and DNA synthesis.
**Usage:**Cyanocobalamin Injection is primarily used for the treatment and prevention of vitamin B12 deficiency, which can occur due to various factors such as inadequate dietary intake, malabsorption syndromes, certain medical conditions, or as a result of certain medications.
The injection is typically administered intramuscularly (into the muscle) or subcutaneously (under the skin) as directed by a healthcare professional. The dosage and frequency of administration may vary depending on the individual's condition, age, and response to treatment. It's important to follow the prescribed dosage and administration instructions provided by the healthcare provider.
**Side Effects:**Like any medication, Cyanocobalamin Injection may cause side effects in some individuals. Common side effects may include:
1. Injection site reactions such as pain, redness, or swelling2. Nausea or vomiting3. Diarrhea4. Headache5. Dizziness6. Itching or rash
These side effects are usually mild and temporary, but if they persist or worsen, it's important to inform a healthcare professional promptly.
In rare cases, some individuals may experience more severe side effects such as allergic reactions (e.g., difficulty breathing, swelling of the face or throat, severe rash), chest pain, rapid heartbeat, or unusual weakness or tiredness. If any of these symptoms occur, immediate medical attention should be sought.
It's important to inform your healthcare provider about any pre-existing medical conditions, allergies, or medications you are taking before starting Cyanocobalamin Injection to minimize the risk of potential adverse effects and ensure safe and effective treatment.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 6-7 days

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**Composition:**Each ampoule of Dexamethasone Sodium Phosphate Injection 4mg contains:
- Dexamethasone Sodium Phosphate: 4mg- Excipients: Sodium Citrate, Sodium Metabisulfite, Water for Injection
**Usage:**Dexamethasone Sodium Phosphate Injection is a corticosteroid medication used for various conditions due to its anti-inflammatory and immunosuppressant properties. It is typically administered via intravenous (IV) or intramuscular (IM) injection. The usage may vary depending on the specific condition being treated, and it should be administered under the supervision of a healthcare professional. Some common uses include:
1. **Allergic Reactions:** Dexamethasone can be used to treat severe allergic reactions, such as anaphylaxis, where rapid suppression of the immune response is necessary.  2. **Inflammatory Conditions:** It is prescribed for a wide range of inflammatory conditions such as rheumatoid arthritis, asthma exacerbations, severe dermatitis, and inflammatory bowel disease.   3. **Autoimmune Disorders:** Dexamethasone is used to manage autoimmune diseases like lupus, where the immune system mistakenly attacks healthy tissues.   4. **Cancer Treatment:** It may be used as part of chemotherapy protocols to reduce inflammation, manage side effects, or enhance the efficacy of other medications.   5. **Cerebral Edema:** Dexamethasone is often used to reduce brain swelling associated with tumors or cerebral trauma.
The dosage and duration of treatment will be determined by the healthcare provider based on the patient's condition, response to treatment, and any underlying health issues.
**Side Effects:**While Dexamethasone Sodium Phosphate can be highly effective in treating various conditions, it may also cause side effects. Common side effects include:
1. **Increased Appetite:** Patients may experience increased hunger and weight gain.  2. **Fluid Retention:** Dexamethasone can cause fluid retention, leading to swelling in the legs and ankles.   3. **Mood Changes:** Some individuals may experience mood swings, irritability, or even depression.   4. **Insomnia:** Difficulty sleeping or insomnia is a common side effect.   5. **Gastrointestinal Issues:** Dexamethasone can irritate the stomach lining, leading to indigestion, nausea, or even gastric ulcers.   6. **Increased Blood Sugar:** It may elevate blood glucose levels, especially in patients with diabetes.   7. **Weakening of Immune System:** While it suppresses inflammation, it can also weaken the immune system, increasing susceptibility to infections.
It's important for patients to report any concerning side effects to their healthcare provider. Long-term or high-dose use of dexamethasone can increase the risk of more severe side effects, including osteoporosis, hypertension, and adrenal insufficiency. Therefore, the medication should be used cautiously and as prescribed by a healthcare professional.

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• Production Capacity: 1000
• Delivery Time: 6-7 days

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**Composition:**Each liquid ampoule of Diclofenac Sodium Injection 75mg/3ml contains 75mg of Diclofenac Sodium as the active ingredient.
**Usage:**Diclofenac Sodium Injection is a nonsteroidal anti-inflammatory drug (NSAID) primarily used to relieve pain and inflammation. It is commonly prescribed for the following conditions:
1. **Pain Relief**: Diclofenac Sodium Injection is often used to alleviate moderate to severe pain associated with conditions such as:   - Postoperative pain   - Renal colic   - Traumatic injury   - Musculoskeletal disorders   - Dental pain
2. **Inflammatory Conditions**: It is effective in reducing inflammation associated with conditions like:   - Rheumatoid arthritis   - Osteoarthritis   - Ankylosing spondylitis   - Acute gout
**Dosage and Administration:**- The dosage of Diclofenac Sodium Injection should be determined by a healthcare professional based on the individual patient's condition, severity of pain or inflammation, and medical history.- It is typically administered via intramuscular or intravenous injection.- The usual recommended dose for adults is 75-150mg per day, divided into two or three doses.- For postoperative pain relief, a single dose of 75mg may be sufficient.- The injection should be administered slowly over a period of at least 2 minutes to minimize the risk of adverse effects.
**Side Effects:**While Diclofenac Sodium Injection is generally well-tolerated, it may cause some side effects. Common side effects include:
1. **Gastrointestinal Effects**:   - Nausea   - Dyspepsia (indigestion)   - Gastric irritation   - Abdominal pain   - Diarrhea
2. **Cardiovascular Effects**:   - Hypertension (high blood pressure)   - Edema (fluid retention)   - Palpitations
3. **Renal Effects**:   - Impaired renal function   - Fluid retention   - Renal failure (rare)
4. **Hepatic Effects**:   - Elevated liver enzymes   - Hepatitis (inflammation of the liver)
5. **Hematological Effects**:   - Anemia   - Thrombocytopenia (low platelet count)   - Leukopenia (low white blood cell count)
6. **Central Nervous System Effects**:   - Headache   - Dizziness   - Drowsiness
7. **Dermatological Effects**:   - Rash   - Pruritus (itching)   - Photosensitivity (increased sensitivity to sunlight)
8. **Other Effects**:   - Injection site reactions (pain, swelling, redness)
**Precautions and Warnings:**- Diclofenac Sodium Injection should not be used in patients with a history of hypersensitivity to NSAIDs or those with active peptic ulcer disease.- It should be used with caution in patients with a history of cardiovascular disease, renal impairment, or hepatic dysfunction.- Prolonged use of NSAIDs, including Diclofenac Sodium Injection, may increase the risk of gastrointestinal bleeding, ulceration, and perforation.- It should be avoided in the last trimester of pregnancy due to the potential risk of fetal harm.- Patients should be monitored regularly for signs of adverse effects, particularly gastrointestinal bleeding, renal dysfunction, and hepatic impairment.
As with any medication, it's important to consult a healthcare professional for proper diagnosis, dosage, and monitoring when using Diclofenac Sodium Injection.

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• Production Capacity: 1000
• Delivery Time: 6-7 Days

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Composition:Each ampoule of Dicyclomine Hydrochloride Injection contains 10mg of Dicyclomine Hydrochloride as the active ingredient. The injection is typically formulated in a sterile liquid solution for intramuscular or intravenous administration.
Usage:Dicyclomine Hydrochloride Injection is primarily used as an antispasmodic medication to relieve smooth muscle spasms in the gastrointestinal tract. It is commonly prescribed for conditions such as irritable bowel syndrome (IBS), colic, and other gastrointestinal disorders associated with cramping and spasms.
The recommended dosage and route of administration may vary depending on the severity of the condition and the individual patient's response. Typically, it is administered by healthcare professionals in a clinical setting. It should not be self-administered without proper medical guidance.
Side Effects:While Dicyclomine Hydrochloride Injection can be effective in relieving gastrointestinal spasms, it may also cause certain side effects. Common side effects may include:
1. Dry mouth2. Blurred vision3. Dizziness or lightheadedness4. Drowsiness5. Difficulty urinating6. Constipation7. Nausea or vomiting
These side effects are usually mild and transient, but if they persist or worsen, medical attention may be required. In rare cases, severe side effects such as allergic reactions (e.g., rash, itching, swelling of the face/tongue/throat, severe dizziness, or trouble breathing) may occur. If any of these symptoms occur, immediate medical attention should be sought.
It's essential to inform your healthcare provider about any pre-existing medical conditions, allergies, or medications you are currently taking before starting Dicyclomine Hydrochloride Injection to minimize the risk of adverse reactions and ensure safe usage.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 6-7 Days

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**Composition:**Each ampoule of Digoxin Injection contains 250 micrograms (0.25 mg) of digoxin in a sterile liquid form. The inactive ingredients may include water for injection and possibly other excipients necessary for stabilization or pH adjustment.
**Usage:**Digoxin Injection is primarily used in the treatment of heart conditions, particularly heart failure and certain types of irregular heartbeats (arrhythmias), such as atrial fibrillation. It belongs to a class of medications called cardiac glycosides, which work by increasing the strength and efficiency of the heart muscle's contractions.
The injection is usually administered intravenously (IV) or intramuscularly (IM) by a healthcare professional in a clinical setting. The dosage and frequency of administration depend on the patient's condition, age, weight, and renal function. 
It's crucial to follow the prescribed dosage regimen and not to self-administer this medication. Regular monitoring of blood levels and heart function parameters may be necessary during treatment.
**Side Effects:**Like any medication, Digoxin Injection can cause side effects, although not everyone will experience them. Common side effects may include:
1. **Nausea and vomiting:** Some patients may experience gastrointestinal disturbances, such as nausea, vomiting, or loss of appetite.2. **Dizziness or headache:** These symptoms may occur, especially during the initial phase of treatment or with dosage adjustments.3. **Visual disturbances:** Digoxin can cause blurred or yellow-tinted vision. In severe cases, it may also lead to visual hallucinations or color vision changes.4. **Irregular heartbeat:** Paradoxically, digoxin, while used to treat arrhythmias, can also cause or exacerbate irregular heartbeats in some patients.5. **Fatigue or weakness:** Some individuals may feel tired or weak, especially if the dosage is too high.6. **Electrolyte imbalance:** Digoxin can affect electrolyte levels in the body, particularly potassium and magnesium. Low potassium levels can increase the risk of digoxin toxicity.
In case of any unusual or severe side effects, it's important to seek medical attention promptly. Additionally, patients should inform their healthcare provider about any pre-existing medical conditions or medications they are taking to avoid potential drug interactions or complications.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 6-7 days

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**Composition:**
Each milliliter of Dopamine Hydrochloride Injection contains 40 mg of dopamine hydrochloride as the active ingredient. The solution is typically prepared in a sterile aqueous solution suitable for injection.
**Usage:**
Dopamine Hydrochloride Injection is primarily used in medical settings for its effects on the cardiovascular system. It is administered intravenously under the supervision of a healthcare professional. The dosage and rate of administration are determined by the patient's condition, response to treatment, and other factors such as age and weight.
1. **Shock**: Dopamine is often used in the treatment of shock, particularly in cases where there is inadequate perfusion of vital organs. It helps to improve cardiac output and blood pressure, thereby restoring tissue perfusion.
2. **Heart Failure**: In cases of acute heart failure, dopamine may be administered to improve cardiac contractility and increase cardiac output.
3. **Renal Failure**: Dopamine may be used in certain cases of acute renal failure to improve renal blood flow and urine output.
**Side Effects:**While dopamine can be beneficial in certain medical situations, it can also cause various side effects, some of which may be serious. These side effects may include:
1. **Tachycardia**: Increased heart rate is a common side effect of dopamine administration.
2. **Arrhythmias**: Irregular heart rhythms may occur with dopamine use, particularly at higher doses.
3. **Hypertension**: Dopamine can increase blood pressure, which may be undesirable in some patients.
4. **Nausea and Vomiting**: Gastrointestinal disturbances such as nausea and vomiting may occur.
5. **Headache**: Some patients may experience headaches during or after dopamine administration.
6. **Palpitations**: Sensations of rapid or irregular heartbeat may occur.
7. **Extravasation**: If the medication leaks into surrounding tissues during administration, it can cause tissue necrosis and damage.
8. **Peripheral Ischemia**: In rare cases, dopamine administration may lead to reduced blood flow to the extremities, causing ischemia or gangrene.
9. **Anxiety and Restlessness**: Some patients may experience increased anxiety or restlessness.
It is crucial for healthcare providers to monitor patients closely during dopamine administration and adjust the dosage as necessary to minimize the risk of adverse effects. Additionally, patients should be informed about potential side effects and instructed to report any concerning symptoms promptly.

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• Production Capacity: 1000
• Delivery Time: 6-7 days

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Composition:Each ampoule contains 10mg of Furosemide as the active ingredient, along with excipients such as sodium chloride, water for injection, and possibly other inactive ingredients.
Usage:Furosemide injection is a diuretic medication used to treat conditions where there is excess fluid accumulation in the body, such as congestive heart failure, liver disease, kidney disease, or edema (swelling). It works by increasing the amount of urine produced by the kidneys, thereby reducing excess fluid and relieving symptoms such as shortness of breath, swelling, and high blood pressure.
The injection is administered intravenously (IV) by a healthcare professional in a hospital or clinical setting. The dosage and frequency of administration depend on the individual's medical condition, response to treatment, and other factors determined by the healthcare provider.
It's crucial to follow the healthcare provider's instructions carefully and not to exceed the prescribed dosage to avoid potential side effects and complications.
Side Effects:While Furosemide is generally considered safe and effective when used as directed, like any medication, it can cause side effects. Common side effects may include:
1. Electrolyte imbalances (such as low levels of potassium, sodium, or magnesium)2. Dehydration3. Dizziness or lightheadedness4. Headache5. Nausea or vomiting6. Muscle cramps or weakness7. Increased urination8. Rash or itching
Rare but more severe side effects may include:
1. Severe allergic reactions (difficulty breathing, rash, itching, swelling of the face, lips, or throat)2. Hearing loss3. Kidney damage or failure4. Liver damage5. Irregular heartbeat
If any of these side effects occur or worsen, it's important to seek medical attention promptly. Additionally, inform your healthcare provider of any other medications or supplements you are taking to avoid potential drug interactions.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 6-7 days

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**Composition:**Each ampoule of Gentamicin Injection contains 40mg of Gentamicin (as sulfate) in a sterile aqueous solution.
**Usage:**Gentamicin Injection is a broad-spectrum antibiotic used primarily to treat bacterial infections. It is administered intramuscularly or intravenously, typically following the directions of a healthcare professional. The dosage and frequency of administration depend on the severity of the infection, the patient's age, weight, renal function, and other factors.
It is essential to follow the prescribed dosage and complete the full course of treatment, even if symptoms improve before the medication is finished. Failure to do so may result in the development of antibiotic resistance or incomplete eradication of the infection.
**Side Effects:**While Gentamicin is effective in treating bacterial infections, it may also cause adverse reactions. Common side effects may include:
1. **Nephrotoxicity:** Gentamicin can cause damage to the kidneys, especially if high doses are administered or if the patient has pre-existing kidney problems. Symptoms of nephrotoxicity may include decreased urine output, swelling in the legs or ankles, and fatigue.
2. **Ototoxicity:** Gentamicin can also affect the inner ear, leading to hearing loss, dizziness, or ringing in the ears (tinnitus). This side effect is usually irreversible and can be more pronounced in patients with pre-existing hearing problems.
3. **Neurotoxicity:** In some cases, Gentamicin can cause neurological side effects, such as numbness, tingling, muscle twitching, or seizures. These effects are more likely to occur at higher doses or with prolonged use.
4. **Allergic Reactions:** Some individuals may experience allergic reactions to Gentamicin, which can range from mild skin rashes to severe anaphylaxis. Symptoms of an allergic reaction may include itching, hives, difficulty breathing, and swelling of the face, lips, or throat.
5. **Superinfection:** Prolonged use of Gentamicin may lead to the overgrowth of non-susceptible bacteria or fungi, resulting in secondary infections.
6. **Other Side Effects:** Other less common side effects may include nausea, vomiting, diarrhea, headache, and fever.
It's essential to report any unusual or severe side effects to a healthcare professional promptly. Additionally, Gentamicin should be used with caution in patients with pre-existing kidney or hearing problems, as well as in infants, elderly individuals, and pregnant or breastfeeding women, under the supervision of a healthcare provider.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 6-7 days

Product Details:

**Composition:**- Heparin Sodium Injection 5000 IU (International Units) per milliliter in liquid form.
**Usage:**- Heparin Sodium Injection is a medication primarily used as an anticoagulant (blood thinner). It works by inhibiting the formation of blood clots. It is commonly used in various medical conditions such as:  - Treatment and prevention of blood clots in veins (deep vein thrombosis) and lungs (pulmonary embolism).  - Prevention of blood clot formation during surgeries, particularly cardiac and orthopedic surgeries.  - Management of certain heart conditions such as atrial fibrillation and heart attacks.  - Treatment of blood clotting disorders like disseminated intravascular coagulation (DIC).
**Dosage:**- Dosage varies based on the patient's medical condition, weight, and response to treatment.- It is administered by injection either into a vein (intravenously) or under the skin (subcutaneously).- Dosage adjustments may be necessary based on regular monitoring of blood clotting parameters.
**Side Effects:**- Common side effects may include:  - Bleeding or bruising at the injection site.  - Nosebleeds.  - Blood in urine or stools.  - Unusual or prolonged bleeding from cuts or wounds.  - Gastrointestinal upset such as nausea or vomiting.  - Skin rash or irritation at the injection site.- Serious side effects which require immediate medical attention may include:  - Signs of internal bleeding such as severe headache, dizziness, weakness, confusion, or slurred speech.  - Allergic reactions such as hives, difficulty breathing, or swelling of the face, lips, tongue, or throat.  - Thrombocytopenia (low platelet count) leading to increased risk of bleeding.  - Osteoporosis (thinning of bones) with long-term use.  - Heparin-induced thrombocytopenia (HIT), a potentially life-threatening complication characterized by a decrease in platelet count and increased risk of blood clot formation.
It's crucial to inform your healthcare provider about any existing medical conditions, allergies, medications (prescription or over-the-counter), and supplements you are taking before starting Heparin Sodium Injection. Additionally, regular monitoring of blood clotting parameters and dosage adjustments as necessary should be conducted under the supervision of a qualified healthcare professional.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 6-7 days

Product Details:

Composition:Each milliliter of Hyoscine Butylbromide Injection contains 20 milligrams of hyoscine butylbromide as the active ingredient.
Usage:Hyoscine Butylbromide Injection is a medication used to relieve symptoms associated with gastrointestinal and genitourinary disorders. It works by relaxing smooth muscles in the digestive and urinary systems, thereby reducing spasms and cramping. It is commonly prescribed for conditions such as irritable bowel syndrome (IBS), colic, bladder spasms, and menstrual cramps.
The injection is administered intramuscularly (into a muscle) or intravenously (directly into a vein) by a healthcare professional. The dosage and frequency of administration will vary depending on the specific condition being treated and the patient's medical history. It is important to follow the instructions provided by the healthcare provider or as indicated on the prescription label.
Side Effects:While Hyoscine Butylbromide is generally well-tolerated, like all medications, it may cause side effects in some individuals. Common side effects may include:
1. Dry mouth2. Blurred vision3. Dizziness or lightheadedness4. Drowsiness5. Constipation6. Urinary retention (difficulty passing urine)7. Allergic reactions such as rash, itching, or swelling of the face, lips, or tongue (seek immediate medical attention if these occur)
Less common but more severe side effects may include:
1. Rapid or irregular heartbeat2. Difficulty breathing3. Confusion or hallucinations4. Severe abdominal pain5. Fever6. Difficulty swallowing
If any of these side effects occur, it is important to seek medical attention promptly. Additionally, patients should inform their healthcare provider of any other medications they are taking, as interactions may occur.
It is important for patients to discuss the potential risks and benefits of Hyoscine Butylbromide Injection with their healthcare provider before starting treatment.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 6-7 days

Product Details:

**Composition:**- Iron Dextran: 50mg per mL (as elemental iron)- Other ingredients: Water for injection, sodium hydroxide (to adjust pH), and/or hydrochloric acid (to adjust pH)
**Usage:**Iron Dextran is administered via intramuscular or intravenous injection by a healthcare professional. The dosage is based on the severity of the anemia and the patient's weight. Typically, it is injected slowly to minimize the risk of adverse reactions. Before administering Iron Dextran, a test dose may be given to check for allergic reactions.
**Side Effects:**1. **Allergic Reactions:** Immediate hypersensitivity reactions can occur, ranging from mild symptoms like rash and itching to severe reactions like anaphylaxis. This is why a test dose is often administered before the full dose.2. **Injection Site Reactions:** Pain, swelling, and irritation at the injection site are common.3. **Systemic Reactions:** Fever, chills, headache, dizziness, nausea, vomiting, and joint or muscle pain may occur.4. **Iron Overload:** Excessive administration of Iron Dextran can lead to iron overload, which may manifest as abdominal pain, joint pain, fatigue, and organ damage.5. **Hypotension:** Intravenous administration can rarely cause a sudden drop in blood pressure.6. **Darkening of Skin:** Prolonged use or high doses of Iron Dextran may cause skin discoloration at the injection site.7. **Thrombophlebitis:** Inflammation of the vein may occur, especially with intravenous administration.
**Precautions:**- Iron Dextran should be used cautiously in patients with a history of allergies, asthma, or other hypersensitivity reactions.- Patients with liver disease, hemoglobinopathies, or chronic inflammatory conditions may require special monitoring.- Regular monitoring of iron levels and hematologic parameters is necessary during treatment.- Iron Dextran should not be used in patients with known hypersensitivity to the drug or in cases of existing iron overload conditions.
It's crucial to discuss the risks and benefits of Iron Dextran therapy with a healthcare professional before starting treatment.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 6-7 days

Product Details:

**Composition:**- **Active Ingredient:** Ketorolac Tromethamine- **Strength:** 30mg per milliliter (30mg/ml)- **Inactive Ingredients:** Typically, the inactive ingredients might include water for injection and/or other excipients necessary for formulation stability and pH adjustment. Specific inactive ingredients can vary depending on the manufacturer.
**Usage:**Ketorolac Tromethamine Injection USP is a nonsteroidal anti-inflammatory drug (NSAID) indicated for the short-term (up to 5 days) management of moderately severe acute pain that requires analgesia at the opioid level. It is typically administered via intravenous or intramuscular routes.
**Dosage:**The dosage and administration of Ketorolac Tromethamine Injection should be individualized based on the patient's needs, pain intensity, and response to therapy. The usual recommended adult dosage is:- For Intravenous (IV) or Intramuscular (IM) Use: 30 mg every 6 hours, not to exceed 120 mg/day. In the elderly, dosage should not exceed 60 mg/day.- For patients weighing less than 50 kg, a lower initial dose of 15 mg may be considered.
It's essential to adhere strictly to the recommended dosage and duration of therapy to minimize the risk of adverse effects.
**Side Effects:**Ketorolac Tromethamine Injection, like other NSAIDs, can be associated with various side effects. Common side effects may include:1. Gastrointestinal Effects: Nausea, vomiting, dyspepsia, diarrhea, abdominal pain, gastrointestinal bleeding, ulceration, and perforation, which can be severe and may lead to fatal outcomes.2. Cardiovascular Effects: Hypertension, edema, and exacerbation of congestive heart failure or other cardiovascular conditions.3. Renal Effects: Decreased renal function, renal insufficiency, renal failure, and interstitial nephritis.4. Hematologic Effects: Anemia, thrombocytopenia, and other hematologic abnormalities.5. Central Nervous System Effects: Headache, dizziness, drowsiness, and confusion.6. Allergic Reactions: Hypersensitivity reactions such as bronchospasm, rash, and anaphylaxis.7. Injection Site Reactions: Pain, redness, and swelling at the injection site.
It's crucial to monitor patients closely for signs of adverse effects, especially in those with a history of gastrointestinal bleeding, peptic ulceration, renal impairment, or those on concurrent therapy with anticoagulants or corticosteroids. If any adverse reactions occur, discontinuation of Ketorolac Tromethamine Injection should be considered, and appropriate therapy initiated as necessary.
Patients should be educated about the potential side effects of Ketorolac Tromethamine Injection, and healthcare providers should weigh the benefits against the risks when prescribing this medication.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 6-7 days

Product Details:

**Composition:**Each milliliter of Labetalol Injection contains 5 milligrams of Labetalol hydrochloride as the active ingredient.
**Usage:**Labetalol Injection is primarily indicated for the management of hypertension (high blood pressure). It is particularly useful in hypertensive emergencies where rapid blood pressure control is essential. The dosage and administration route should be determined by a healthcare professional based on the patient's condition and response to treatment.
**Dosage and Administration:**The dosage of Labetalol Injection varies depending on the severity of hypertension and the patient's individual response. It is typically administered intravenously (IV), and the rate of infusion should be carefully controlled to avoid abrupt changes in blood pressure. Close monitoring of blood pressure and heart rate is necessary during administration. Dosage adjustments may be required based on the patient's clinical response.
**Side Effects:**Labetalol, like any medication, may cause side effects. Common side effects include:
1. **Hypotension (low blood pressure):** Labetalol can cause a decrease in blood pressure, which may lead to symptoms such as dizziness, lightheadedness, or fainting.
2. **Bradycardia (slow heart rate):** Labetalol can slow down the heart rate, resulting in symptoms like fatigue, weakness, or shortness of breath.
3. **Fatigue:** Some patients may experience fatigue or tiredness while taking Labetalol.
4. **Dizziness:** Dizziness is a common side effect of Labetalol, especially when standing up from a sitting or lying position.
5. **Nausea and vomiting:** Some individuals may experience gastrointestinal discomfort, including nausea and vomiting.
6. **Headache:** Headaches can occur as a side effect of Labetalol treatment.
7. **Peripheral edema:** Swelling in the extremities, known as peripheral edema, may occur in some patients.
8. **Bronchospasm:** Labetalol may cause bronchospasm in individuals with asthma or other respiratory conditions.
9. **Heart block:** In rare cases, Labetalol can cause heart block, a condition where the electrical signals in the heart are disrupted, leading to abnormal heart rhythms.
10. **Allergic reactions:** Serious allergic reactions to Labetalol, although rare, can occur. Symptoms may include rash, itching, swelling, severe dizziness, or trouble breathing.
It is important to report any unusual or severe side effects to a healthcare professional promptly. Additionally, patients should not discontinue Labetalol abruptly without consulting their healthcare provider, as sudden withdrawal can lead to rebound hypertension or other complications.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 6-7 days

Product Details:

**Composition:**Each 1 mL ampoule of Levetiracetam Injection contains:- Levetiracetam: XX mg (specify the concentration per mL)- Inactive ingredients: (list any inactive ingredients present in the formulation)
**Usage:**Levetiracetam Injection is indicated as adjunctive therapy in the treatment of:- Partial onset seizures in adults and pediatric patients 1 month of age and older with epilepsy.- Myoclonic seizures in adults and adolescents 12 years of age and older with juvenile myoclonic epilepsy.- Primary generalized tonic-clonic seizures in adults and adolescents 12 years of age and older with idiopathic generalized epilepsy.
The dosage and administration of Levetiracetam Injection should be individualized according to patient's age, weight, renal function, and therapeutic response. It is administered intravenously either as a bolus injection or as an infusion. Dosage adjustments may be necessary in patients with renal impairment.
**Side Effects:**Common side effects of Levetiracetam Injection may include:- Dizziness- Somnolence- Weakness- Infection- Nervousness- Loss of coordination- Fatigue- Hostility- Aggression- Anemia- Thrombocytopenia- Leukopenia- Elevated liver enzymes
Less common but more severe side effects may include:- Severe allergic reactions (rash, hives, itching, difficulty breathing, swelling of the face, lips, tongue, or throat)- Suicidal thoughts or actions- Mood or behavior changes- Depression- New or worsening seizures
It is essential to inform healthcare providers of any unusual side effects experienced while using Levetiracetam Injection. Patients should not discontinue the medication abruptly without consulting a healthcare professional.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 6-7 days

Product Details:

**Composition:**Each ampoule of Lidocaine Injection 20mg contains:- Active Ingredient: Lidocaine Hydrochloride 20mg- Excipients: Sodium Chloride, Water for Injection
**Usage:**Lidocaine Injection is a local anesthetic medication used for various purposes, including:1. Local anesthesia for minor surgical procedures.2. Nerve block for pain management during medical procedures.3. As an adjunct in regional anesthesia techniques.4. Treatment of ventricular arrhythmias (in higher doses and under medical supervision).5. Topical anesthesia for mucous membranes and minor burns (when appropriately diluted).
**Dosage and Administration:**- The dosage of Lidocaine Injection varies depending on the procedure, patient's weight, and medical condition.- It is administered by healthcare professionals trained in local anesthesia techniques.- The injection is typically given subcutaneously, intramuscularly, or via nerve blocks.- Dosage adjustments may be necessary in elderly patients or those with hepatic or cardiac impairment.
**Side Effects:**Lidocaine Injection, like any medication, may cause side effects. Common side effects include:1. Localized reactions at the injection site such as redness, swelling, or pain.2. Numbness or tingling at the site of injection.3. Dizziness or lightheadedness.4. Nausea or vomiting.5. Headache.6. Blurred vision.7. Tremors or muscle twitching.
**Rare but serious side effects may include:**1. Allergic reactions such as hives, itching, or difficulty breathing.2. Bradycardia (slow heart rate) or arrhythmias.3. Hypotension (low blood pressure).4. Seizures or convulsions.5. Neurological symptoms such as confusion or agitation.
**Precautions:**- Lidocaine Injection should be used with caution in patients with a known allergy to local anesthetics.- Patients with heart conditions or liver impairment should be closely monitored during Lidocaine administration.- Lidocaine should be used cautiously in patients with epilepsy or a history of seizures.- The dosage should be carefully adjusted in elderly patients or those with renal impairment.- Lidocaine should not be used in regions with compromised circulation or in areas of infection.
**Note:**This information serves as a general guideline. Always consult a healthcare professional for proper diagnosis, dosage, and administration of Lidocaine Injection, taking into account individual patient factors and medical history.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 6-7 days

Product Details:

Composition:Each mL of Methylprednisolone Acetate Injection contains 40 mg of methylprednisolone acetate as the active ingredient. The injection is typically provided in a sterile liquid form.
Usage:Methylprednisolone Acetate Injection is a corticosteroid medication used to treat various inflammatory conditions, allergic reactions, autoimmune diseases, and certain types of cancers. It works by reducing inflammation and suppressing the immune system's response.
This injection is usually administered by a healthcare professional into a muscle or joint, depending on the condition being treated. The dosage and frequency of administration will vary depending on the severity of the condition and the individual's response to the treatment. It's essential to follow the prescribed dosage and administration instructions provided by your healthcare provider.
Side Effects:Like all medications, Methylprednisolone Acetate Injection can cause side effects, although not everyone experiences them. Common side effects may include:
1. Injection site reactions such as pain, redness, or swelling.2. Nausea or vomiting.3. Headache.4. Dizziness.5. Changes in mood or behavior, including irritability or agitation.6. Insomnia or difficulty sleeping.7. Increased appetite and weight gain.8. Fluid retention, leading to swelling in the hands, feet, or ankles.9. Increased risk of infections due to suppression of the immune system.10. Elevated blood sugar levels, which can worsen diabetes or lead to the development of new-onset diabetes.11. Osteoporosis or bone thinning with long-term use.12. Increased susceptibility to cataracts or glaucoma.
Rare but serious side effects may also occur, including severe allergic reactions, adrenal insufficiency, or worsening of underlying conditions such as peptic ulcer disease or psychiatric disorders. If you experience any severe or persistent side effects, contact your healthcare provider immediately.
It's crucial to weigh the potential benefits of treatment with Methylprednisolone Acetate Injection against the risks of side effects, especially with long-term or high-dose use. Your healthcare provider will monitor you closely while you are receiving this medication to minimize the risk of adverse effects and adjust your treatment plan as needed.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 6-7 days

Product Details:

**Composition:**Each ampoule of Metoclopramide Injection contains 10mg of Metoclopramide Hydrochloride as the active ingredient. The injection is formulated in a liquid form suitable for intravenous or intramuscular administration.
**Usage:**Metoclopramide Injection is primarily used for the following indications:
1. **Nausea and Vomiting:** It is often used to manage nausea and vomiting associated with various conditions such as chemotherapy, radiation therapy, surgery, gastroenteritis, and migraine headaches.
2. **Gastroparesis:** Metoclopramide Injection is also indicated for the treatment of gastroparesis, a condition characterized by delayed emptying of the stomach contents into the small intestine, leading to symptoms such as nausea, vomiting, bloating, and early satiety.
3. **Facilitation of Gastrointestinal Procedures:** In some cases, it may be used to facilitate certain gastrointestinal procedures such as small bowel intubation.
The dosage and administration of Metoclopramide Injection should be individualized based on the patient's condition, age, weight, and response to treatment. It is usually administered by healthcare professionals either intravenously or intramuscularly.
**Side Effects:**While Metoclopramide Injection is generally well-tolerated, it may cause some side effects. Common side effects include:
1. **Drowsiness:** Patients may experience drowsiness or sedation, especially at higher doses or with prolonged use. Caution should be exercised when driving or operating machinery.
2. **Extrapyramidal Symptoms (EPS):** This includes symptoms such as dystonia (involuntary muscle contractions), akathisia (restlessness), parkinsonism (tremors, rigidity), and tardive dyskinesia (involuntary movements of the face and limbs). These symptoms are more common with higher doses and prolonged use.
3. **Hyperprolactinemia:** Metoclopramide can increase prolactin levels, which may lead to symptoms such as breast tenderness, gynecomastia (enlargement of breast tissue in males), and menstrual irregularities in females.
4. **Gastrointestinal Effects:** Some patients may experience diarrhea, constipation, abdominal pain, or gastrointestinal discomfort.
5. **Hypotension:** In rare cases, Metoclopramide can cause a decrease in blood pressure, especially when administered rapidly intravenously.
6. **Allergic Reactions:** Allergic reactions such as rash, itching, swelling, or difficulty breathing may occur in some individuals.
Patients should be monitored for these side effects, and appropriate measures should be taken if they occur. In case of severe or persistent side effects, healthcare professionals should be consulted immediately.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 6-7 days

Product Details:

**Composition:**Each liquid ampoule of Nandrolone Decanoate Injection contains 50mg of Nandrolone Decanoate as the active ingredient.
**Usage:**Nandrolone Decanoate is an anabolic steroid commonly used to treat various medical conditions such as anemia, osteoporosis, and wasting syndromes. It is administered via intramuscular injection.
The dosage and frequency of administration depend on the specific medical condition being treated and the individual patient's response to the treatment. It is crucial to follow the instructions provided by a healthcare professional or as directed on the product label.
**Side Effects:**While Nandrolone Decanoate can be beneficial for treating certain medical conditions, it may also cause several side effects. Common side effects may include:
1. **Androgenic Effects:** Nandrolone Decanoate is derived from testosterone and can exhibit androgenic properties. This may lead to acne, oily skin, increased body hair growth, and scalp hair loss.
2. **Cardiovascular Effects:** Prolonged use of Nandrolone Decanoate may increase the risk of cardiovascular issues such as high blood pressure, heart palpitations, and increased cholesterol levels.
3. **Hepatotoxicity:** Excessive use or misuse of Nandrolone Decanoate may cause liver damage or dysfunction. It is essential to monitor liver function regularly during treatment.
4. **Endocrine Disruption:** Nandrolone Decanoate can disrupt normal hormone production in the body, leading to potential adverse effects such as testicular atrophy, menstrual irregularities, and gynecomastia (enlargement of male breast tissue).
5. **Psychological Effects:** Some users may experience mood swings, irritability, aggression, or other changes in behavior while using Nandrolone Decanoate.
6. **Masculinization in Women:** Female users may develop masculine characteristics such as deepening of the voice, enlargement of the clitoris, and disruption of the menstrual cycle.
7. **Virilization in Children:** In children, Nandrolone Decanoate can cause premature closure of growth plates, leading to stunted growth. It should be used cautiously in pediatric patients and only under the guidance of a healthcare professional.
8. **Injection Site Reactions:** Pain, swelling, or redness at the injection site may occur, especially with frequent injections.
It is important to note that the above list is not exhaustive, and other side effects may occur. Individuals using Nandrolone Decanoate should discuss any concerns or adverse reactions with their healthcare provider promptly. Additionally, misuse or abuse of this medication can lead to serious health complications and should be avoided.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 6-7 days

Product Details:

**Composition:**Each ampoule of Nikethamide Injection contains 375 mg of Nikethamide in 1.5 ml of liquid.
**Usage:**Nikethamide is a medication primarily used as a respiratory stimulant. It is commonly prescribed to treat conditions associated with respiratory depression or inadequate ventilation, such as drug overdose, anesthesia-induced respiratory depression, or certain types of poisoning. 
The injection is administered intravenously or intramuscularly by a healthcare professional. Dosage and frequency of administration should be determined by a qualified medical practitioner based on the patient's condition and response to treatment.
**Side Effects:**While Nikethamide is generally well-tolerated, like any medication, it may cause side effects in some individuals. Common side effects may include:
1. Nausea2. Vomiting3. Headache4. Dizziness5. Flushing or warmth sensation at the injection site6. Sweating7. Rapid heartbeat (tachycardia)8. Hypersensitivity reactions (rash, itching, swelling)
It's important to report any unusual or severe side effects to a healthcare professional promptly. In rare cases, Nikethamide may cause more serious adverse reactions, and immediate medical attention should be sought if any concerning symptoms arise.
This information is provided for informational purposes only and should not be used as a substitute for professional medical advice. Always consult a healthcare provider for guidance on the appropriate use, dosage, and potential risks associated with medication.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 6-7 days

Product Details:

**Composition:**Each milliliter (ml) of Noradrenaline Injection contains 1 milligram (mg) of Noradrenaline Bitartrate. 
**Usage:**Noradrenaline Injection is primarily used in medical emergencies such as shock (caused by severe blood loss, infection, heart attack, or severe allergic reaction) to increase blood pressure and improve blood flow to vital organs. It acts by stimulating alpha-adrenergic receptors, resulting in vasoconstriction (narrowing of blood vessels), which leads to an increase in blood pressure.
**Dosage and Administration:**- The dosage of Noradrenaline Injection varies based on the individual's condition, weight, and response to the medication.- It is administered intravenously (into a vein) by healthcare professionals, typically through a continuous infusion pump to maintain a desired blood pressure level.- Dosage adjustments may be necessary based on the patient's response and vital signs.
**Side Effects:**- Common side effects may include:  - Increased blood pressure  - Headache  - Nausea  - Vomiting  - Anxiety  - Difficulty sleeping (insomnia)  - Pale skin  - Cold extremities- Serious side effects that require immediate medical attention may include:  - Severe high blood pressure (hypertensive crisis)  - Irregular heartbeat (arrhythmias)  - Difficulty breathing  - Chest pain  - Severe headache  - Sudden weakness or numbness on one side of the body  - Fainting or dizziness- Allergic reactions to Noradrenaline Injection are rare but may include symptoms such as rash, itching, swelling, severe dizziness, or trouble breathing.
**Precautions:**- Noradrenaline Injection should be used cautiously in patients with certain medical conditions such as heart disease, high blood pressure, diabetes, hyperthyroidism, or pheochromocytoma.- It should not be used in patients with hypovolemic shock (shock due to low blood volume) unless adequate fluid replacement has been provided.- Close monitoring of blood pressure, heart rate, and urine output is essential during Noradrenaline therapy.- Noradrenaline Injection should be administered only by healthcare professionals trained in its use and who have experience in managing patients with shock.
**Storage:**- Store Noradrenaline Injection at room temperature (20-25°C / 68-77°F), protected from light and moisture.- Keep it out of the reach of children.
This information is a general guide and should not replace professional medical advice. Always consult a healthcare provider for personalized recommendations regarding medication usage and potential side effects.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 6-7 days

Product Details:

**Composition:**Each ampoule of Potassium Chloride Injection Concentrate contains 100mg of potassium chloride as the active ingredient, along with sterile water for injection as the vehicle.
**Usage:**Potassium Chloride Injection Concentrate is primarily used for the treatment and prevention of potassium deficiency (hypokalemia) in patients who are unable to take potassium orally or in cases where rapid correction of potassium levels is necessary. It may be administered intravenously or diluted and given by slow intravenous infusion under medical supervision.
Dosage and administration should be determined by a healthcare professional based on the individual patient's condition, potassium levels, and response to treatment. It is crucial to follow the prescribed dosage and administration instructions carefully to avoid complications.
**Side Effects:**While Potassium Chloride Injection Concentrate is essential for correcting potassium imbalances, it can potentially cause adverse effects, especially if administered incorrectly or in excessive doses. Common side effects may include:
1. Nausea and vomiting2. Abdominal discomfort or pain3. Diarrhea4. Irritation or burning sensation at the injection site5. Electrolyte disturbances, including hyperkalemia (high potassium levels), especially if administered too rapidly or in high doses6. Cardiac arrhythmias (irregular heart rhythms), particularly in patients with pre-existing heart conditions or impaired renal function7. Muscle weakness or paralysis8. Allergic reactions, including itching, rash, or swelling at the injection site (rare)
Patients receiving Potassium Chloride Injection Concentrate should be closely monitored for signs of electrolyte imbalance, cardiac abnormalities, or allergic reactions. In case of any concerning symptoms or adverse reactions, medical attention should be sought promptly.
It is important for healthcare professionals to consider the patient's medical history, concurrent medications, and overall health status before administering Potassium Chloride Injection Concentrate to minimize the risk of adverse effects and ensure safe and effective treatment.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 6-7 days

Product Details:

**Composition:**Each ampoule of Promethazine hydrochloride Injection contains 25mg of promethazine hydrochloride as the active ingredient.
**Usage:**
Promethazine hydrochloride Injection is a medication primarily used to treat various conditions such as nausea, vomiting, motion sickness, and allergic reactions. It belongs to a class of drugs known as phenothiazines, which exert their effects by blocking certain neurotransmitters in the brain.
The injection form of promethazine is typically reserved for situations where oral administration is not feasible or when rapid onset of action is required. It may be administered intramuscularly (into the muscle) or intravenously (directly into a vein) under the supervision of a healthcare professional.
The dosage and frequency of administration should be determined by a healthcare provider based on the individual's condition, age, and response to treatment.
**Side Effects:**
While Promethazine hydrochloride Injection can be effective in managing various symptoms, it may also cause certain side effects. Common side effects may include:
1. Drowsiness or sedation2. Dizziness3. Blurred vision4. Dry mouth5. Constipation6. Urinary retention7. Low blood pressure8. Injection site reactions such as pain or irritation
Less commonly, more serious side effects may occur, including:
1. Extrapyramidal symptoms such as tremors, muscle stiffness, or involuntary movements2. Neuroleptic malignant syndrome (a rare but serious condition characterized by fever, muscle rigidity, altered mental status, and autonomic dysfunction)3. Severe allergic reactions4. Respiratory depression (especially when administered rapidly or in high doses)
It's important to inform a healthcare provider promptly if any side effects occur, particularly if they are severe or persistent. Additionally, individuals with certain medical conditions or those taking other medications should exercise caution and discuss the risks and benefits of Promethazine hydrochloride Injection with their healthcare provider before use.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 6-7 days

Product Details:

**Composition:**
Sodium bicarbonate injection 7.5% w/v ampoule contains the active ingredient sodium bicarbonate, which is a white, crystalline powder with the chemical formula NaHCO₃. Each milliliter of the injection solution contains 75 mg of sodium bicarbonate.
**Usage:**
1. **Acidosis Treatment:** Sodium bicarbonate injection is primarily used to treat metabolic acidosis, a condition where there is an imbalance in the body's acid-base levels, leading to a decrease in blood pH. It works by neutralizing excess acid in the blood, helping to restore a normal pH balance.
2. **Electrolyte Replacement:** In some cases, sodium bicarbonate injection may be administered to replenish electrolytes, particularly sodium and bicarbonate ions, in individuals experiencing electrolyte imbalances.
3. **Treatment of Certain Drug Toxicities:** Sodium bicarbonate may also be used as an adjunctive treatment in cases of drug overdose, particularly those involving drugs that can lead to metabolic acidosis.
4. **Adjunctive Therapy:** Additionally, it may be used as adjunctive therapy in certain medical procedures or conditions where metabolic alkalosis needs to be corrected.
**Side Effects:**
1. **Metabolic Alkalosis:** Overuse or improper administration of sodium bicarbonate injection can lead to metabolic alkalosis, a condition characterized by elevated blood pH levels. This can result in symptoms such as confusion, muscle twitching, nausea, vomiting, and tingling sensations.
2. **Fluid Overload:** Administration of sodium bicarbonate injection can lead to fluid overload, particularly in patients with compromised kidney function or congestive heart failure. Symptoms of fluid overload may include swelling, shortness of breath, and increased blood pressure.
3. **Hypernatremia:** Excessive administration of sodium bicarbonate can lead to elevated sodium levels in the blood (hypernatremia), which can cause symptoms such as excessive thirst, confusion, and muscle twitching.
4. **Hypokalemia:** Sodium bicarbonate administration can lead to potassium depletion (hypokalemia) in some individuals, especially if used for prolonged periods or in high doses. Symptoms of hypokalemia include muscle weakness, fatigue, and irregular heart rhythms.
5. **Local Irritation:** Injection site reactions such as pain, redness, or swelling may occur at the site of administration.
6. **Allergic Reactions:** While rare, allergic reactions to sodium bicarbonate injection can occur, leading to symptoms such as rash, itching, swelling, or difficulty breathing.
It is important to administer sodium bicarbonate injection under the supervision of a healthcare professional and to closely monitor patients for any adverse reactions. Dosage and frequency of administration should be determined based on the individual patient's condition and needs.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 6-7 days

Product Details:

**Composition:**
Sterile Water for Injection is a sterile, nonpyrogenic preparation of water for injection which contains no bacteriostat, antimicrobial agent, or added buffer. It is provided in single-dose containers.
**Usage:**
Sterile Water for Injection is used for various medical purposes, including:
1. **Dilution of Medications:** It is used to dilute medications for intravenous administration when prescribed by a healthcare professional.2. **Wound Irrigation:** It can be used for wound irrigation to clean wounds and facilitate healing.3. **Reconstitution of Powders:** Some medications come in a powdered form that needs to be reconstituted before administration. Sterile Water for Injection is used to dissolve these powders into a solution suitable for injection.4. **Laboratory Procedures:** It is used in laboratory procedures where sterile water is required.
**Side Effects:**
Since Sterile Water for Injection is composed solely of water and does not contain any active ingredients, it is generally considered safe when used as directed. However, misuse or contamination of the solution can lead to adverse effects. Some potential risks include:
1. **Infection:** If the solution becomes contaminated, it can introduce bacteria or other pathogens into the body, leading to infection.2. **Hypotonicity:** Sterile Water for Injection is hypotonic, meaning it has a lower concentration of solutes compared to body fluids. In rare cases, rapid infusion of large volumes of hypotonic solutions can lead to hemolysis (rupture of red blood cells) and electrolyte imbalances.3. **Allergic Reactions:** Although rare, some individuals may be allergic to components used in the manufacturing process or may develop allergic reactions to contaminants present in the solution.4. **Tissue Damage:** If injected incorrectly or inappropriately, Sterile Water for Injection can cause tissue damage or irritation at the injection site.
It's important for healthcare professionals to follow proper procedures for handling and administering Sterile Water for Injection to minimize the risk of adverse effects. Patients should also be informed about the potential risks and monitored closely during administration.

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• Production Capacity: 1000
• Delivery Time: 6-7 days

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**Composition:**Each ampoule of Thiamine hydrochloride (Vitamin B1) Injection contains 100 mg of Thiamine hydrochloride as the active ingredient.
**Usage:**Thiamine hydrochloride injection is primarily used to treat or prevent thiamine (vitamin B1) deficiency, which can occur due to various conditions such as alcoholism, malnutrition, gastrointestinal disorders, and certain medical treatments. Thiamine is essential for the proper functioning of the nervous system, muscles, and heart.
The injection is administered either intravenously (IV), intramuscularly (IM), or subcutaneously (SC) as directed by a healthcare professional. Dosage and frequency of administration depend on the individual's condition and response to treatment. It is important to follow the prescribed dosage and regimen strictly.
**Side Effects:**Common side effects of Thiamine hydrochloride injection may include:
1. Injection site reactions such as pain, redness, or swelling2. Nausea or vomiting3. Allergic reactions such as itching, rash, or hives4. Flushing or sweating5. Feeling of warmth or tingling sensation6. Dizziness or lightheadedness
Serious side effects are rare but may include severe allergic reactions (anaphylaxis) characterized by difficulty breathing, swelling of the face, lips, tongue, or throat, and severe dizziness.
It is essential to report any unusual or severe side effects to your healthcare provider promptly. Additionally, inform your healthcare provider about any pre-existing medical conditions or medications you are taking to avoid potential interactions or complications.

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• Production Capacity: 1000
• Delivery Time: 6-7 days

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**Composition:**
Tranexamic acid is a synthetic derivative of the amino acid lysine. Each injection contains 100mg of tranexamic acid as the active ingredient.
**Usage:**
Tranexamic acid injection is commonly used for the following medical purposes:
1. **Bleeding Disorders:** It is often prescribed to control or prevent excessive bleeding in conditions such as hemophilia, von Willebrand disease, and other clotting disorders.
2. **Surgery:** Tranexamic acid may be administered before, during, or after surgical procedures to reduce blood loss and the need for transfusions, particularly in orthopedic, cardiac, and gynecological surgeries.
3. **Menstrual Disorders:** For women with heavy menstrual bleeding (menorrhagia), tranexamic acid can help to lessen blood loss and alleviate associated symptoms.
4. **Dental Procedures:** It may be used in dental surgeries to minimize bleeding during or after procedures like tooth extractions or periodontal surgeries.
5. **Trauma:** Tranexamic acid has shown efficacy in reducing bleeding in trauma patients, particularly in cases of traumatic injury or during resuscitation efforts.
**Side Effects:**
Although generally well-tolerated, tranexamic acid injection may cause some side effects in certain individuals. Common side effects include:
1. **Nausea and Vomiting:** Some individuals may experience gastrointestinal discomfort, including nausea and vomiting, particularly when higher doses are administered.
2. **Headache:** Headaches are a common side effect reported by patients receiving tranexamic acid.
3. **Dizziness:** Tranexamic acid can occasionally cause dizziness or lightheadedness.
4. **Muscle Cramps:** Some individuals may experience muscle cramps or muscle weakness.
5. **Fatigue:** Feelings of tiredness or fatigue may occur in some patients.
6. **Allergic Reactions:** Although rare, allergic reactions such as rash, itching, swelling, or difficulty breathing may occur. Immediate medical attention is necessary if any signs of an allergic reaction develop.
7. **Thrombosis:** There have been rare reports of blood clot formation (thrombosis) associated with tranexamic acid use, particularly in patients with a history of thrombotic events or those at increased risk of clotting disorders.
It's important to note that this list is not exhaustive, and individuals should consult with their healthcare provider for personalized advice regarding the use of tranexamic acid injection and to discuss any potential side effects or concerns.

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• Production Capacity: 1000
• Delivery Time: 6-7 days

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Composition:Each 1 milliliter (mL) of triamcinolone acetonide injection typically contains 40 milligrams (mg) of triamcinolone acetonide as the active ingredient. Other components may include preservatives and stabilizers to maintain the stability and sterility of the solution.
Usage:Triamcinolone acetonide injection is administered by healthcare professionals, usually in a clinical setting. The dosage and frequency of injections depend on the specific condition being treated, the severity of symptoms, and the individual patient's response to the medication.
Common uses of triamcinolone acetonide injection include:
1. Allergic Reactions: Triamcinolone acetonide injection can be used to treat severe allergic reactions, such as anaphylaxis, where rapid and potent anti-inflammatory action is required to alleviate symptoms like swelling, itching, and respiratory distress.
2. Arthritis: In cases of severe arthritis, particularly rheumatoid arthritis or osteoarthritis, where systemic inflammation leads to joint pain, swelling, and stiffness, triamcinolone acetonide injection may be prescribed to reduce inflammation and relieve symptoms.
3. Inflammatory Bowel Disease (IBD): Triamcinolone acetonide injection can be part of the treatment regimen for patients with inflammatory bowel diseases like Crohn's disease or ulcerative colitis, where inflammation of the gastrointestinal tract leads to symptoms such as abdominal pain, diarrhea, and rectal bleeding.
4. Dermatological Conditions: Certain severe skin conditions, such as psoriasis, eczema, or severe allergic dermatitis, may require systemic treatment with triamcinolone acetonide injection to reduce inflammation and alleviate symptoms like itching, redness, and scaling.
5. Respiratory Disorders: Triamcinolone acetonide injection may be used in the management of severe respiratory conditions, including asthma exacerbations or chronic obstructive pulmonary disease (COPD) exacerbations, to reduce airway inflammation and improve breathing.
Side Effects:While triamcinolone acetonide injection can be highly effective in treating various medical conditions, it is associated with potential side effects, especially when used long-term or at high doses. Common side effects may include:
1. Increased Risk of Infections: Corticosteroids like triamcinolone acetonide can suppress the immune system, increasing the risk of developing infections. Patients should be monitored for signs of infection, and precautions should be taken to prevent exposure to contagious illnesses.
2. Glucose Intolerance and Diabetes: Triamcinolone acetonide injection can cause elevated blood sugar levels, leading to glucose intolerance or exacerbation of diabetes in susceptible individuals. Regular monitoring of blood glucose levels is necessary, especially in diabetic patients.
3. Osteoporosis: Prolonged use of corticosteroids like triamcinolone acetonide can weaken bones and increase the risk of osteoporosis, particularly in postmenopausal women and elderly patients. Adequate calcium and vitamin D intake, along with bone density monitoring, may be recommended.
4. Adrenal Suppression: Long-term use of triamcinolone acetonide injection can suppress the natural production of cortisol by the adrenal glands, leading to adrenal insufficiency. Abrupt discontinuation of the medication can precipitate adrenal crisis in some cases.
5. Fluid Retention and Edema: Corticosteroids can cause sodium and water retention, leading to fluid retention and edema, especially in susceptible individuals like those with congestive heart failure or hypertension.
6. Mood Changes and Psychiatric Effects: Some patients may experience mood swings, anxiety, depression, or other psychiatric effects while taking triamcinolone acetonide injection, particularly at higher doses or with prolonged use.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 6-7 days

Product Details:

**Composition:**
Each milliliter of the Vitamin B-Complex Injection contains the following active ingredients:
1. Thiamine Hydrochloride (Vitamin B1): 100 mg2. Pyridoxine Hydrochloride (Vitamin B6): 100 mg3. Cyanocobalamin (Vitamin B12): 100 mcg
Inactive ingredients may include sterile water for injection, sodium hydroxide or hydrochloric acid for pH adjustment, and possibly preservatives or stabilizers.
**Usage:**
Vitamin B-Complex injections are typically administered intramuscularly (IM) or intravenously (IV) under medical supervision. The specific dosage and frequency of administration depend on the individual's health condition, age, and other factors. However, a common dosage regimen may include:
- Adults: 1 mL injected intramuscularly once daily or as directed by a healthcare professional.- Children: Dosage should be determined by a pediatrician based on weight and medical condition.
It's crucial to follow the instructions provided by the healthcare provider or pharmacist. Never self-administer injections without proper medical guidance.
Vitamin B-Complex injections are commonly prescribed for the treatment or prevention of various conditions associated with Vitamin B deficiencies, such as:
1. Peripheral neuropathy2. Megaloblastic anemia3. Diabetic neuropathy4. Vitamin B deficiencies due to certain medical conditions or dietary restrictions
Additionally, they may be used as a supplement for individuals who have difficulty absorbing nutrients orally, such as those with gastrointestinal disorders.
**Side Effects:**
While Vitamin B-Complex injections are generally considered safe when administered properly, they may cause side effects in some individuals. Common side effects include:
1. Injection site reactions: Pain, swelling, or redness at the injection site.2. Allergic reactions: Rarely, some individuals may experience allergic reactions such as itching, hives, rash, or difficulty breathing. Seek immediate medical attention if you experience any allergic symptoms.3. Nausea or vomiting: Some individuals may experience gastrointestinal discomfort after receiving the injection.4. Hypersensitivity reactions: In rare cases, hypersensitivity reactions such as anaphylaxis may occur, which require immediate medical intervention.
It's essential to inform your healthcare provider if you experience any unexpected or severe side effects after receiving a Vitamin B-Complex injection. Additionally, individuals with certain medical conditions or allergies should consult their healthcare provider before starting any new medication or supplement regimen.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 6-7 days

Product Details:

**Composition:**Hydroxocobalamin Injection 1000mcg contains hydroxocobalamin as its active ingredient. Each milliliter of the injection solution typically contains 1000 micrograms (mcg) of hydroxocobalamin. Hydroxocobalamin is a form of vitamin B12 and is used to treat vitamin B12 deficiency.
**Usage:**Hydroxocobalamin Injection 1000mcg is administered intramuscularly (IM) or intravenously (IV) by a healthcare professional. The dosage and frequency of administration depend on the patient's condition, severity of deficiency, and the doctor's prescription. Generally, it is given as a series of injections over a specific period, followed by maintenance doses as needed. 
Hydroxocobalamin is primarily used to treat vitamin B12 deficiency, which can occur due to various reasons including inadequate dietary intake, malabsorption syndromes, certain medications, or certain medical conditions such as pernicious anemia. It helps replenish vitamin B12 levels in the body, which is essential for the proper functioning of nerves, cells, and DNA synthesis.
**Side Effects:**While Hydroxocobalamin Injection is generally considered safe when administered under the supervision of a healthcare professional, it may cause some side effects in certain individuals. Common side effects may include:
1. Injection site reactions such as pain, redness, or swelling.2. Nausea or vomiting.3. Headache.4. Dizziness.5. Diarrhea.6. Itching or rash.
Serious side effects are rare but may include allergic reactions such as difficulty breathing, swelling of the face, lips, tongue, or throat, severe dizziness, or fainting. 
It's important to promptly report any unusual or severe symptoms to a healthcare provider. Additionally, patients with a history of allergies or hypersensitivity to hydroxocobalamin or cobalt should inform their healthcare provider before receiving the injection.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 6-7 days

Product Details:

Composition:Tobramycin Injection contains Tobramycin as its active ingredient. Each mL of the injection typically contains 40 milligrams of Tobramycin.
Usage:Tobramycin Injection is commonly prescribed to treat various bacterial infections, particularly those caused by susceptible strains of Gram-negative organisms. It is often used in severe infections where other antibiotics may not be effective. Tobramycin works by inhibiting bacterial protein synthesis, thereby killing susceptible bacteria.
This medication is usually administered intravenously or intramuscularly by a healthcare professional in a hospital or clinical setting. The dosage and duration of treatment are determined by the severity of the infection, the patient's age, weight, renal function, and other factors. It is essential to follow the healthcare provider's instructions carefully and complete the full course of treatment even if symptoms improve before completion.
Side Effects:While Tobramycin is effective in treating bacterial infections, it may also cause certain side effects. Some common side effects of Tobramycin Injection include:
1. Nausea and vomiting2. Diarrhea3. Headache4. Dizziness5. Skin rash or itching6. Injection site reactions (such as pain, redness, or swelling)7. Kidney damage or dysfunction (especially with prolonged use or high doses)8. Hearing loss or ringing in the ears (tinnitus) - particularly with high doses or prolonged therapy
Serious side effects such as allergic reactions, severe dizziness, difficulty breathing, or signs of kidney damage (such as changes in urine output or unusual tiredness) should be reported to a healthcare professional immediately.
It is important for patients to inform their healthcare provider about any pre-existing medical conditions, allergies, or medications they are taking before starting Tobramycin treatment to minimize the risk of adverse effects and drug interactions.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 6-7 days

Product Details:

Composition:L-Ornithine-L-Aspartate Infusion contains the active ingredients L-ornithine and L-aspartate, each at a concentration of 5mg/ml.
Usage:L-Ornithine-L-Aspartate Infusion is typically administered intravenously under the supervision of a healthcare professional. The dosage and duration of treatment will be determined by the prescribing physician based on the patient's condition, medical history, and response to therapy.
This infusion is commonly used in the management of hepatic encephalopathy, a condition characterized by impaired brain function due to liver disease. L-Ornithine-L-Aspartate works by promoting the detoxification of ammonia in the liver, thereby reducing its levels in the bloodstream and alleviating symptoms associated with hepatic encephalopathy.
Side Effects:While L-Ornithine-L-Aspartate Infusion is generally well-tolerated, like any medication, it may cause side effects in some individuals. Common side effects may include:
1. Nausea2. Vomiting3. Diarrhea4. Headache5. Dizziness6. Allergic reactions (such as rash, itching, or swelling)
In rare cases, severe allergic reactions or adverse effects on liver function may occur. Patients should report any unusual or concerning symptoms to their healthcare provider promptly.
It's important to note that this is not an exhaustive list of side effects. Patients should discuss any concerns or potential side effects with their healthcare provider before starting treatment with L-Ornithine-L-Aspartate Infusion.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 6-7 days

Product Details:

**Composition:**
Quinine Dihydrochloride Injection 250mg contains quinine dihydrochloride as the active ingredient. Quinine is an alkaloid derived from the bark of the cinchona tree. Each milliliter of the injection contains 250mg of quinine dihydrochloride.
**Usage:**
Quinine Dihydrochloride Injection 250mg is primarily used for the treatment of malaria, a serious and potentially life-threatening parasitic infection caused by Plasmodium species. It is often used in cases where oral therapy is not feasible or when rapid onset of action is required.
The injection is administered intravenously under medical supervision. The dosage and duration of treatment are determined by the severity of the infection, the patient's age, weight, and overall health condition, as well as the specific strain of malaria.
It is crucial to follow the healthcare provider's instructions regarding the administration of the injection and complete the full course of treatment as prescribed, even if symptoms improve before the course is completed.
**Side Effects:**
Quinine Dihydrochloride Injection 250mg may cause some adverse effects, which can vary in severity from mild to serious. Common side effects may include:
1. Nausea2. Vomiting3. Abdominal pain4. Diarrhea5. Headache6. Dizziness7. Ringing in the ears (tinnitus)8. Changes in vision
Serious side effects are rare but may include:
1. Allergic reactions such as rash, itching, or swelling of the face, lips, or tongue2. Irregular heartbeat (arrhythmia)3. Low blood sugar levels (hypoglycemia)4. Hemolytic uremic syndrome (a disorder that affects the blood and blood vessels, leading to kidney failure)5. Severe skin reactions such as Stevens-Johnson syndrome or toxic epidermal necrolysis
It is essential to seek medical attention immediately if any severe side effects occur. Patients should inform their healthcare provider of any unexpected or bothersome side effects experienced during treatment.
**Precautions:**
Before using Quinine Dihydrochloride Injection 250mg, patients should inform their healthcare provider about any pre-existing medical conditions, allergies, or medications they are taking, including over-the-counter drugs and herbal supplements.
Quinine injection should be used with caution in patients with a history of heart rhythm disorders, glucose-6-phosphate dehydrogenase (G6PD) deficiency, kidney or liver disease, or myasthenia gravis.
Pregnant or breastfeeding women should consult their healthcare provider before using this medication, as it may pose risks to the fetus or nursing infant.
Patients should avoid consuming alcohol while undergoing treatment with quinine, as it may increase the risk of adverse effects.
Quinine Dihydrochloride Injection 250mg should be stored as per the manufacturer's instructions, away from moisture, heat, and light, and out of reach of children.
This medication should only be used under the supervision of a qualified healthcare professional in a clinical setting, where appropriate monitoring and supportive care are available.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 6-7 days

Product Details:

**Composition:**
Enoxaparin Sodium Injection contains the active ingredient enoxaparin sodium, which is a low molecular weight heparin (LMWH). Each 0.4 ml pre-filled syringe contains 40 mg of enoxaparin sodium.
**Usage:**
Enoxaparin Sodium Injection is commonly prescribed for the following conditions:
1. **Deep Vein Thrombosis (DVT):** It is used for the prevention and treatment of deep vein thrombosis, which can lead to conditions such as pulmonary embolism.
2. **Pulmonary Embolism (PE):** It can also be used in the treatment of pulmonary embolism, where blood clots travel to the lungs.
3. **Acute Coronary Syndrome (ACS):** Enoxaparin is often used as part of the treatment regimen for acute coronary syndrome, including unstable angina and myocardial infarction (heart attack).
4. **Prevention of Clotting During Hemodialysis:** Enoxaparin may also be used to prevent blood clotting during hemodialysis in patients with kidney problems.
5. **Prevention of Clots in Certain Surgical Procedures:** It is sometimes prescribed to prevent blood clots in patients undergoing certain types of surgeries, particularly orthopedic surgeries such as hip or knee replacement.
**Side Effects:**
While enoxaparin sodium is generally well-tolerated, some individuals may experience side effects. Common side effects include:
1. **Bleeding:** Since enoxaparin is an anticoagulant, it can increase the risk of bleeding. This may manifest as nosebleeds, bleeding gums, easy bruising, or prolonged bleeding from cuts.
2. **Injection Site Reactions:** Some people may experience pain, redness, or swelling at the injection site.
3. **Hematoma Formation:** In some cases, enoxaparin injections may lead to the formation of hematomas (localized collection of blood outside blood vessels) at the injection site.
4. **Thrombocytopenia:** A decrease in platelet count, known as thrombocytopenia, is a rare but serious side effect of enoxaparin therapy.
5. **Allergic Reactions:** Although rare, some individuals may experience allergic reactions to enoxaparin sodium, which may manifest as rash, itching, or difficulty breathing.
6. **Osteoporosis:** Prolonged use of enoxaparin may increase the risk of osteoporosis, particularly in patients receiving high doses for an extended period.
7. **Elevated Liver Enzymes:** In some cases, enoxaparin therapy may cause transient elevations in liver enzyme levels, which usually resolve upon discontinuation of the medication.
It's essential to report any unusual or severe side effects to your healthcare provider promptly. Additionally, individuals on enoxaparin therapy should be closely monitored for signs of bleeding and other adverse reactions.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 6-7 DAYS