Dry Injections

Product Details:

**Composition:**Each vial contains Aciclovir sodium equivalent to 250 mg of Aciclovir.
**Usage:**Aciclovir sodium for injection is a medication primarily used in the treatment of certain viral infections, particularly those caused by the herpes simplex virus (HSV) and varicella-zoster virus (VZV). It is administered intravenously under the supervision of a healthcare professional. The dosage and duration of treatment may vary depending on the severity of the infection, the patient's medical history, and other factors determined by the treating physician.
**Indications:**1. Herpes simplex infections: Aciclovir sodium for injection is indicated for the treatment of initial and recurrent episodes of genital herpes and herpes labialis (cold sores).2. Varicella-zoster infections: It is also used in the treatment of chickenpox (varicella) and herpes zoster (shingles) in immunocompromised patients.
**Side Effects:**Like all medications, Aciclovir sodium for injection may cause side effects in some individuals. Common side effects may include:1. Nausea and vomiting2. Headache3. Diarrhea4. Rash5. Fatigue6. Elevated liver enzymes7. Injection site reactions (e.g., pain, redness, swelling)
Rare but potentially serious side effects may include:1. Allergic reactions (e.g., rash, itching, swelling of the face, tongue, or throat, difficulty breathing)2. Kidney problems (e.g., decreased urine output, swelling in the ankles/feet, unusual tiredness)3. Neurological symptoms (e.g., confusion, hallucinations, seizures)4. Blood disorders (e.g., anemia, leukopenia, thrombocytopenia)
It is important to promptly inform a healthcare provider if any side effects occur during treatment. Additionally, patients should be advised to report any unusual symptoms or reactions to their healthcare provider immediately.
**Precautions:**1. Aciclovir sodium for injection should be used with caution in patients with kidney impairment, as dosage adjustments may be necessary.2. Patients should stay adequately hydrated during treatment to help prevent kidney-related side effects.3. It is essential to inform the healthcare provider about any other medications, supplements, or herbal remedies being taken concurrently, as they may interact with Aciclovir.4. This medication should be used with caution during pregnancy and breastfeeding, and the potential risks and benefits should be discussed with a healthcare provider.5. Aciclovir may cause dizziness or drowsiness. Patients should avoid activities that require mental alertness until they know how this medication affects them.6. Patients with a history of hypersensitivity to Aciclovir or valacyclovir should not use this medication.
As with any medication, Aciclovir sodium for injection should only be used under the guidance and supervision of a qualified healthcare professional.

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

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Composition:Artesunate injection contains 60 mg of the active ingredient, artesunate, which is a semi-synthetic derivative of artemisinin, a compound extracted from the plant Artemisia annua.
Usage:Artesunate injection is primarily used in the treatment of severe malaria infections caused by Plasmodium falciparum, including cases of cerebral malaria. It is administered intravenously in a hospital or clinical setting under the supervision of a healthcare professional. 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 healthcare provider's judgment.
Side Effects:While artesunate is generally well-tolerated, like all medications, it may cause side effects in some individuals. Common side effects of artesunate injection may include:
1. Nausea and vomiting2. Dizziness or lightheadedness3. Headache4. Muscle or joint pain5. Diarrhea6. Abdominal pain7. Fatigue or weakness8. Skin rash or itching
Rare but serious side effects may include:
1. Allergic reactions such as difficulty breathing, swelling of the face, lips, tongue, or throat, and hives2. Changes in blood cell counts, leading to anemia, leukopenia, or thrombocytopenia3. Liver dysfunction or hepatotoxicity, presenting as jaundice, dark urine, or abdominal pain4. Electrolyte imbalances5. Neurological symptoms such as confusion, seizures, or loss of consciousness
It's important for patients to promptly report any unusual or severe side effects to their healthcare provider. Additionally, individuals with a history of allergies, liver disease, or other medical conditions should inform their healthcare provider before starting treatment with artesunate injection.

Additional Information:

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

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Composition:Azithromycin for Injection USP 500 mg contains the active ingredient azithromycin, which belongs to the class of medications known as macrolide antibiotics. Each vial typically contains 500 mg of azithromycin as a lyophilized powder for reconstitution.
Usage:Azithromycin for Injection is primarily indicated for the treatment of infections caused by susceptible bacteria. It is commonly prescribed for:
1. Respiratory Tract Infections: Azithromycin is effective against bacterial infections of the lungs and airways, including pneumonia, bronchitis, and exacerbations of chronic obstructive pulmonary disease (COPD).
2. Skin and Soft Tissue Infections: It can be used to treat bacterial infections of the skin, such as cellulitis, impetigo, and erysipelas.
3. Sexually Transmitted Infections (STIs): Azithromycin is sometimes prescribed for the treatment of certain STIs, such as chlamydia and gonorrhea.
4. Other Infections: It may also be used for the treatment of other bacterial infections, including sinusitis, otitis media (ear infections), and certain types of bacterial gastroenteritis.
Dosage and Administration:The dosage and administration of Azithromycin for Injection should be determined by a healthcare professional based on the specific infection being treated, the patient's age and weight, and other factors. It is typically administered intravenously (IV) by a healthcare provider in a hospital or clinical setting. The reconstituted solution should be administered slowly over a period of at least 60 minutes to minimize the risk of infusion-related reactions.
Side Effects:While Azithromycin for Injection is generally well-tolerated, it can cause side effects in some individuals. Common side effects may include:
1. Gastrointestinal Upset: Nausea, vomiting, diarrhea, and abdominal pain are common side effects of azithromycin therapy. These symptoms are usually mild and temporary.
2. Allergic Reactions: Some individuals may experience allergic reactions to azithromycin, which can manifest as rash, itching, swelling of the face or throat, or difficulty breathing. Severe allergic reactions (anaphylaxis) are rare but can be life-threatening and require immediate medical attention.
3. Cardiac Effects: Azithromycin may prolong the QT interval on electrocardiogram (ECG), which can increase the risk of arrhythmias (irregular heart rhythms), particularly in patients with pre-existing cardiac conditions or those taking other medications that also prolong the QT interval.
4. Liver Dysfunction: In rare cases, azithromycin can cause liver damage, leading to elevated liver enzymes and potentially hepatitis.
5. Other Side Effects: Additional side effects may include headache, dizziness, fatigue, and changes in taste or smell.
Precautions and Warnings:Before using Azithromycin for Injection, patients should inform their healthcare provider about any allergies, medical conditions, or medications they are taking, especially other antibiotics, antacids, and medications that affect heart rhythm.
Patients should complete the full course of azithromycin therapy as prescribed by their healthcare provider, even if they start to feel better before the medication is finished. Skipping doses or stopping treatment prematurely can lead to the development of antibiotic-resistant bacteria and recurrent infections.
In conclusion, Azithromycin for Injection is a potent antibiotic used to treat a variety of bacterial infections. While generally safe and effective, it can cause side effects in some individuals, and caution should be exercised when using it, especially in patients with underlying medical conditions or those taking other medications. Patients should follow their healthcare provider's instructions carefully and report any adverse reactions promptly for proper management.

Additional Information:

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

Product Details:

**Composition:**
Aztreonam for Injection 500mg contains the active ingredient aztreonam, which is a monobactam antibiotic. Each vial of Aztreonam for Injection contains 500mg of aztreonam.
**Usage:**
Aztreonam is primarily used to treat bacterial infections caused by susceptible organisms. It is particularly effective against Gram-negative bacteria, including Pseudomonas aeruginosa and Escherichia coli. Aztreonam works by inhibiting the synthesis of bacterial cell walls, ultimately leading to bacterial cell death.
This medication is typically administered intravenously (IV) or intramuscularly (IM) under the supervision of a healthcare professional. The dosage and frequency of administration will depend on various factors such as the severity of the infection, the patient's age, weight, and renal function, as well as the specific organism causing the infection. It's essential to follow the dosage regimen prescribed by your healthcare provider and to complete the full course of treatment, even if symptoms improve before the medication is finished.
**Side Effects:**
Like all medications, Aztreonam for Injection can cause side effects, although not everyone will experience them. Common side effects may include:
1. Nausea and vomiting2. Diarrhea3. Headache4. Injection site reactions (pain, redness, swelling)
Less commonly, Aztreonam may cause more severe side effects. If you experience any of the following, contact your healthcare provider immediately:
1. Severe diarrhea (potentially indicating a Clostridium difficile infection)2. Allergic reactions, including rash, itching, swelling of the face, lips, or tongue, difficulty breathing, or severe dizziness3. Signs of liver problems, such as persistent nausea/vomiting, abdominal pain, yellowing of the eyes or skin (jaundice), dark urine4. Signs of kidney problems, such as decreased urination, swelling in the ankles/feet, unusual tiredness
It's essential to report any unusual symptoms or side effects to your healthcare provider promptly. Additionally, inform your healthcare provider about any other medications you are taking, including prescription, over-the-counter, and herbal supplements, as they may interact with Aztreonam.
Do not use Aztreonam for Injection if you have a known allergy to aztreonam or any other ingredients in the formulation. Always consult your healthcare provider for personalized advice regarding the use of this medication.

Additional Information:

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

Product Details:

**Composition:**Capreomycin for Injection 1000mg is a medication primarily composed of capreomycin sulfate, an antibiotic belonging to the class of medications known as aminoglycosides. Each vial of Capreomycin for Injection 1000mg contains 1000 milligrams (mg) of capreomycin sulfate as the active ingredient.
**Usage:**Capreomycin for Injection 1000mg is typically used in the treatment of multidrug-resistant tuberculosis (MDR-TB), particularly when other first-line medications have failed. It is usually administered as part of a combination therapy regimen under the guidance of a healthcare professional specialized in the treatment of tuberculosis.
The dosage and duration of treatment with Capreomycin for Injection 1000mg may vary depending on factors such as the severity of the infection, the patient's age and weight, and their overall health condition. It is usually administered intramuscularly (into the muscle) or intravenously (into the vein) by a healthcare provider.
It is important to complete the full course of treatment as prescribed by the healthcare provider, even if symptoms improve before the treatment is finished, to prevent the development of drug-resistant strains of tuberculosis.
**Side Effects:**Like all medications, Capreomycin for Injection 1000mg may cause side effects, although not everyone experiences them. Some common side effects of Capreomycin may include:
1. **Nephrotoxicity:** Capreomycin can cause kidney damage, leading to decreased kidney function. Symptoms of nephrotoxicity may include decreased urine output, swelling in the legs or feet, and changes in urine color or frequency. Regular monitoring of kidney function through laboratory tests is essential during treatment.
2. **Ototoxicity:** Capreomycin can cause damage to the inner ear, leading to hearing loss or ringing in the ears (tinnitus). This side effect may be irreversible. It is important to report any changes in hearing or ringing in the ears to a healthcare provider promptly.
3. **Neurotoxicity:** Some individuals may experience neurotoxic effects such as dizziness, vertigo, or muscle weakness while taking Capreomycin. If these symptoms occur, medical attention should be sought immediately.
4. **Injection Site Reactions:** Pain, redness, or swelling at the injection site may occur with intramuscular administration of Capreomycin.
5. **Allergic Reactions:** In rare cases, Capreomycin may cause allergic reactions such as rash, itching, swelling of the face, lips, or tongue, or difficulty breathing. These reactions require immediate medical attention.
It is important to notify a healthcare provider if any side effects occur while taking Capreomycin for Injection 1000mg. They can provide guidance on managing side effects or adjusting the treatment regimen if necessary.

Additional Information:

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

Product Details:

**Composition:**Chloramphenicol Sodium Succinate for Injection typically contains the active ingredient chloramphenicol sodium succinate, which is a broad-spectrum antibiotic. Each vial of 1000mg of Chloramphenicol Sodium Succinate for Injection usually contains chloramphenicol sodium succinate equivalent to 1000mg of chloramphenicol.
**Usage:**Chloramphenicol Sodium Succinate for Injection is primarily indicated for the treatment of serious bacterial infections caused by susceptible strains. It is often reserved for infections where other antibiotics are ineffective or contraindicated.
Some common indications for the use of Chloramphenicol Sodium Succinate for Injection include:
1. Severe bacterial infections such as meningitis, septicemia, and brain abscesses.2. Typhoid fever and other serious systemic infections caused by susceptible organisms.3. Certain types of pneumonia, particularly when caused by bacteria resistant to other antibiotics.
The dosage and duration of treatment with Chloramphenicol Sodium Succinate for Injection should be determined by a qualified healthcare professional based on factors such as the severity of the infection, the patient's age and weight, renal function, and any underlying health conditions.
**Side Effects:**While Chloramphenicol Sodium Succinate for Injection can be effective in treating bacterial infections, it is associated with various side effects, ranging from mild to severe. Some potential side effects include:
1. **Bone marrow suppression:** Chloramphenicol can inhibit bone marrow function, leading to decreased production of red blood cells, white blood cells, and platelets. This can result in anemia, leukopenia, thrombocytopenia, or aplastic anemia.2. **Hypersensitivity reactions:** Some individuals may develop allergic reactions to chloramphenicol, which can manifest as rash, itching, swelling, or rarely, anaphylaxis.3. **Gastrointestinal disturbances:** Nausea, vomiting, diarrhea, and abdominal pain are common side effects of Chloramphenicol Sodium Succinate for Injection.4. **Gray baby syndrome:** This is a rare but serious side effect primarily seen in newborns and infants. It is characterized by abdominal distension, vomiting, cyanosis, and cardiovascular collapse.5. **Neurotoxicity:** High doses or prolonged use of chloramphenicol can lead to neurotoxicity, resulting in symptoms such as headache, confusion, hallucinations, and seizures.
It's important for patients to be monitored closely for signs of adverse reactions while receiving treatment with Chloramphenicol Sodium Succinate for Injection. Any unusual symptoms should be reported to a healthcare provider promptly. Additionally, the use of Chloramphenicol Sodium Succinate for Injection should be avoided in patients with a history of hypersensitivity to chloramphenicol or a previous adverse reaction to the drug.

Additional Information:

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

Product Details:

**Composition:**- Active Ingredient: Colistimethate sodium- Inactive Ingredients: May vary depending on the formulation and brand, but typically include substances such as mannitol or sodium hydroxide for pH adjustment.
**Usage:**- Colistimethate sodium is usually administered intravenously or intramuscularly.- Dosage and duration of treatment depend on the severity of the infection, patient's weight, renal function, and other factors.- It's important to follow the dosage instructions provided by a healthcare professional.
**Indications:**- Colistimethate sodium is indicated for the treatment of infections caused by susceptible strains of Gram-negative bacteria, including Pseudomonas aeruginosa, Acinetobacter spp., and Enterobacteriaceae (e.g., Klebsiella, Escherichia coli) resistant to other antibiotics.
**Side Effects:**- Common side effects may include:  - Nausea  - Vomiting  - Diarrhea  - Stomach pain  - Injection site reactions (pain, redness, swelling)  - Kidney damage or dysfunction (especially with prolonged use or high doses)  - Neurotoxicity (rare, but may manifest as dizziness, confusion, numbness, or tingling sensations)
- Serious side effects may include:  - Allergic reactions (rash, itching, swelling, difficulty breathing)  - Severe diarrhea (potentially indicating Clostridium difficile-associated diarrhea, which can be life-threatening)  - Neuromuscular blockade (rare but serious muscle weakness or paralysis)  - Respiratory depression (especially in patients with compromised respiratory function)
- Patients should seek medical attention if they experience any severe or persistent side effects.
It's crucial to use colistimethate sodium under the guidance of a healthcare professional and to report any adverse reactions promptly. Additionally, due to its potential for nephrotoxicity and neurotoxicity, close monitoring of renal function and neurological status is often necessary during treatment.

Additional Information:

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

Product Details:

**Composition:**Doxycycline for Injection USP contains the active ingredient Doxycycline Hyclate, which is a broad-spectrum antibiotic belonging to the tetracycline class. Each vial typically contains 100 mg of doxycycline hyclate as a lyophilized powder for reconstitution.
**Usage:**Doxycycline for Injection is primarily indicated for the treatment of serious infections caused by susceptible strains of gram-positive and gram-negative bacteria, as well as certain other microorganisms. It is commonly used in the management of severe respiratory tract infections, urinary tract infections, skin and soft tissue infections, and certain sexually transmitted diseases such as chlamydia and gonorrhea. It may also be used as adjunctive therapy in severe acne vulgaris.
The dosage and duration of treatment with Doxycycline for Injection should be determined by a healthcare professional based on the severity of the infection, the patient's age and weight, renal function, and the susceptibility of the causative microorganism. It is usually administered intravenously over a prescribed period, as directed by a healthcare provider.
**Side Effects:**While Doxycycline for Injection is generally well-tolerated, like all medications, it can cause side effects in some individuals. Common side effects may include:
1. Gastrointestinal disturbances such as nausea, vomiting, diarrhea, or abdominal pain.2. Esophageal irritation or ulceration, particularly if the medication is not taken with an adequate amount of water and/or if the patient lies down shortly after administration.3. Photosensitivity reactions, leading to sunburn-like symptoms upon exposure to sunlight or ultraviolet (UV) light.4. Skin rash or itching.5. Oral or vaginal candidiasis (yeast infection) due to disruption of normal microbial flora.6. Headache or dizziness.7. Transient elevation of liver enzymes.
Rare but potentially serious side effects may include severe allergic reactions (e.g., anaphylaxis), severe skin reactions (e.g., Stevens-Johnson syndrome, toxic epidermal necrolysis), intracranial hypertension (pseudotumor cerebri), and Clostridium difficile-associated diarrhea (CDAD), which may range from mild diarrhea to life-threatening colitis.
Patients should be advised to report any unexpected or severe side effects to their healthcare provider promptly. It's important to note that prolonged or unnecessary use of antibiotics like doxycycline can lead to the development of bacterial resistance and may reduce the effectiveness of future treatment options. Therefore, the medication should only be used as prescribed and for the duration recommended by a healthcare professional.

Additional Information:

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

Product Details:

Composition:Esomeprazole for injection 40mg contains the active ingredient esomeprazole, which is a proton pump inhibitor (PPI). Each vial typically contains esomeprazole sodium as the active ingredient, along with excipients to maintain stability and facilitate administration.
Usage:Esomeprazole for injection is primarily indicated for the treatment of various gastrointestinal conditions where oral therapy is not feasible or appropriate. These conditions may include:
1. Gastroesophageal Reflux Disease (GERD): Esomeprazole injection is used for the short-term treatment of GERD in patients who are unable to take oral medication or require rapid symptom relief.
2. Peptic Ulcer Disease: It is indicated for the short-term treatment of peptic ulcers, including duodenal ulcers, gastric ulcers, and stress ulcers, in patients who are unable to take oral therapy.
3. Zollinger-Ellison Syndrome: Esomeprazole injection may be used in the management of Zollinger-Ellison syndrome, a rare condition characterized by excessive gastric acid secretion, when oral treatment is not feasible.
Dosage and Administration:The dosage of esomeprazole for injection 40mg should be determined by a healthcare professional based on the patient's condition, severity of symptoms, and response to treatment. It is typically administered intravenously over a specified period, usually 10 to 30 minutes, depending on the specific indication and the patient's clinical status.
Side Effects:While esomeprazole for injection is generally well-tolerated, like any medication, it may cause adverse effects in some individuals. Common side effects associated with esomeprazole injection may include:
1. Headache2. Nausea3. Abdominal pain4. Diarrhea5. Dizziness6. Fatigue
Rare but serious side effects may also occur, including:
1. Allergic reactions such as rash, itching, or swelling of the face, tongue, or throat2. Severe gastrointestinal disorders such as Clostridium difficile-associated diarrhea3. Hypomagnesemia (low magnesium levels), which may manifest as muscle spasms, seizures, or abnormal heart rhythms
It is essential for patients to promptly report any unusual or severe symptoms to their healthcare provider.
Precautions and Warnings:Before using esomeprazole for injection, patients should inform their healthcare provider about any medical conditions they have, including allergies, liver disease, or osteoporosis. Additionally, patients should disclose all medications they are taking, including prescription, over-the-counter, and herbal supplements, to avoid potential drug interactions.
Pregnant or breastfeeding women should use esomeprazole injection with caution, as its safety in these populations has not been established conclusively.
Patients should not exceed the recommended dosage or duration of treatment without consulting their healthcare provider. Prolonged use of PPIs may increase the risk of certain complications, including fractures, vitamin B12 deficiency, and kidney damage.
In conclusion, esomeprazole for injection 40mg is a potent medication used for the short-term treatment of various gastrointestinal conditions when oral therapy is not feasible or appropriate. While generally safe and effective, it may cause side effects in some individuals, and patients should be closely monitored by healthcare professionals during treatment.

Additional Information:

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

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**Composition:**Glutathione injection typically contains 600 mg of glutathione, which is a tripeptide composed of three amino acids: cysteine, glutamic acid, and glycine. Glutathione is naturally produced in the body and plays a crucial role in various physiological processes, including detoxification, antioxidant defense, and immune function.
**Usage:**Glutathione injections are commonly used for various purposes, including skin lightening, anti-aging, liver detoxification, and immune system support. The dosage and frequency of injections can vary depending on the individual's needs and the advice of a healthcare professional.
1. **Skin Lightening**: Glutathione is often used for its skin-lightening effects. It is believed to inhibit melanin production, leading to a lighter complexion. However, the effectiveness of glutathione for skin lightening is still a subject of debate, and results may vary among individuals.
2. **Anti-Aging**: Glutathione is a powerful antioxidant that helps neutralize free radicals and reduce oxidative stress, which can contribute to aging. By reducing oxidative damage, glutathione may help slow down the aging process and promote youthful skin.
3. **Liver Detoxification**: The liver is the body's primary detoxification organ, and glutathione plays a crucial role in supporting its detoxification functions. Glutathione helps remove toxins and harmful substances from the body, protecting the liver from damage and promoting overall health.
4. **Immune System Support**: Glutathione also plays a vital role in supporting the immune system. It helps enhance the activity of immune cells, such as T cells and natural killer cells, which are essential for fighting infections and diseases.
**Side Effects:**While glutathione injections are generally considered safe for most people when used as directed, they may cause side effects in some individuals. Common side effects may include:
1. **Skin Reactions**: Some individuals may experience skin reactions at the injection site, such as redness, itching, or swelling. These reactions are usually mild and temporary.
2. **Allergic Reactions**: In rare cases, glutathione injections may trigger allergic reactions in sensitive individuals. Symptoms of an allergic reaction may include hives, itching, difficulty breathing, or swelling of the face, lips, tongue, or throat. Immediate medical attention is necessary if an allergic reaction occurs.
3. **Nausea and Digestive Issues**: Some people may experience nausea, vomiting, or digestive discomfort after receiving glutathione injections. These symptoms are usually mild and transient.
4. **Headache and Dizziness**: Glutathione injections may occasionally cause headache, dizziness, or lightheadedness in some individuals. These symptoms typically resolve on their own without intervention.
5. **Injection Site Reactions**: Injection site reactions such as pain, bruising, or inflammation may occur, especially if the injection is administered improperly.
It's essential to consult with a healthcare professional before starting glutathione injections, especially if you have any underlying health conditions or are taking medications. Additionally, it's crucial to follow the recommended dosage and administration guidelines to minimize the risk of side effects. If you experience any severe or persistent side effects after receiving glutathione injections, seek medical attention promptly.

Additional Information:

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

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Composition:- Hydrocortisone sodium succinate: 100 mg (active ingredient)- Other ingredients: (may vary depending on the specific formulation and brand)
Usage:Hydrocortisone sodium succinate for injection is a corticosteroid medication used for various medical conditions, including but not limited to:
1. **Inflammatory Conditions:** It is used to treat inflammation associated with conditions such as rheumatoid arthritis, lupus, psoriasis, and inflammatory bowel disease.2. **Allergic Reactions:** Hydrocortisone sodium succinate may be administered to manage severe allergic reactions, including anaphylaxis.3. **Endocrine Disorders:** It is used in the management of adrenal insufficiency (Addison's disease) where the body does not produce enough cortisol.4. **Shock:** Hydrocortisone sodium succinate may be given as a part of the treatment for shock, especially in cases of septic shock or adrenal crisis.
Dosage and administration should be determined by a healthcare professional and may vary based on the individual patient's condition, response to treatment, and other factors.
Side Effects:While hydrocortisone sodium succinate can be effective in treating various conditions, it can also cause several side effects, including:
1. **Immune System Suppression:** Prolonged use or high doses of hydrocortisone sodium succinate can suppress the immune system, increasing the risk of infections.2. **Fluid Retention:** This medication can cause sodium and water retention, leading to edema (swelling) and increased blood pressure.3. **Glucose Intolerance:** Hydrocortisone can interfere with glucose metabolism, leading to elevated blood sugar levels, especially in individuals with diabetes.4. **Osteoporosis:** Long-term use of corticosteroids like hydrocortisone can lead to bone thinning and an increased risk of fractures.5. **Gastrointestinal Effects:** Common gastrointestinal side effects include stomach irritation, ulceration, and bleeding.6. **Psychiatric Effects:** Corticosteroids can cause mood changes, insomnia, and in some cases, psychiatric disorders such as depression or anxiety.7. **Adrenal Suppression:** Prolonged use of hydrocortisone can suppress the body's natural production of cortisol, leading to adrenal insufficiency when the medication is stopped abruptly.8. **Skin Changes:** Side effects such as thinning of the skin, easy bruising, and increased susceptibility to infections can occur with long-term use.
It's important for patients to be monitored regularly by their healthcare provider while using hydrocortisone sodium succinate to manage any potential side effects and adjust the dosage as needed. Additionally, patients should be educated about the risks and benefits of the medication and instructed on proper administration techniques.

Additional Information:

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

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**Composition:**Kanamycin Injection contains Kanamycin sulfate as the active ingredient. Each milliliter of the injection solution typically contains either 1000 mg or 100 mg of Kanamycin sulfate, depending on the concentration.
**Usage:**Kanamycin Injection is an antibiotic medication used to treat various bacterial infections. It belongs to the aminoglycoside class of antibiotics and works by inhibiting bacterial protein synthesis, thereby halting the growth and spread of the bacteria causing the infection. 
It is typically administered intravenously (IV) or intramuscularly (IM) by a healthcare professional. The dosage and frequency of administration depend on the severity of the infection, the patient's age, weight, and overall health condition. It is essential to follow the dosage instructions provided by the healthcare provider or as mentioned on the prescription label.
**Side Effects:**While Kanamycin Injection is effective in treating bacterial infections, it may cause some side effects. These side effects may vary in severity and occurrence from person to person. Common side effects of Kanamycin Injection include:
1. **Nausea and vomiting:** Some patients may experience nausea and vomiting, particularly during the initial stages of treatment. This can usually be managed by taking the medication with food or adjusting the dosage.
2. **Dizziness or lightheadedness:** Kanamycin Injection may cause dizziness or a feeling of lightheadedness in some individuals. It is advisable to avoid driving or operating heavy machinery if you experience these symptoms.
3. **Rash or itching:** Allergic reactions to Kanamycin Injection may manifest as skin rashes or itching. If you notice any skin changes or itching after receiving the injection, inform your healthcare provider immediately.
4. **Kidney damage:** Prolonged or excessive use of Kanamycin Injection may lead to kidney damage. Patients with pre-existing kidney conditions or those receiving high doses of the medication are at a higher risk. Regular monitoring of kidney function is necessary during treatment.
5. **Hearing loss:** Kanamycin Injection has been associated with hearing loss, particularly in patients receiving high doses or prolonged treatment. This side effect may be irreversible in some cases. Patients experiencing any changes in hearing should report it to their healthcare provider promptly.
6. **Neurotoxicity:** In rare cases, Kanamycin Injection may cause neurotoxicity, leading to symptoms such as numbness, tingling, muscle twitching, or seizures. Prompt medical attention is necessary if any neurological symptoms occur.
7. **Digestive disturbances:** Some patients may experience diarrhea or abdominal discomfort while taking Kanamycin Injection. It is essential to stay hydrated and inform your healthcare provider if these symptoms persist.
It is crucial to report any unexpected or severe side effects to your healthcare provider promptly. Additionally, do not discontinue the medication without consulting your doctor, even if you experience side effects.

Additional Information:

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

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Composition:Each vial of Methylprednisolone Sodium Succinate for Injection USP contains 125mg of Methylprednisolone Sodium Succinate as the active ingredient.
Usage:Methylprednisolone Sodium Succinate is a corticosteroid medication used to treat various conditions such as allergic reactions, inflammation, autoimmune diseases, and certain types of cancers. It works by reducing inflammation and suppressing the immune system's response. This medication is typically administered intravenously (into a vein) by a healthcare professional. The dosage and frequency of administration depend on the specific condition being treated and the individual's response to the medication. It's important to follow the dosage instructions provided by your healthcare provider.
Side Effects:While Methylprednisolone Sodium Succinate can be effective in treating various conditions, it may also cause some side effects. Common side effects may include:
1. Increased appetite2. Weight gain3. Fluid retention4. Elevated blood pressure5. Mood changes, such as irritability or agitation6. Difficulty sleeping7. Increased risk of infections8. Impaired wound healing9. Changes in blood sugar levels10. Osteoporosis (weakening of the bones)11. Muscle weakness12. Stomach irritation or ulcers13. Skin thinning or bruising14. Cataracts or glaucoma (with long-term use)
It's important to notify your healthcare provider if you experience any side effects while using Methylprednisolone Sodium Succinate. Some side effects may require medical attention, while others may resolve on their own as your body adjusts to the medication. Your healthcare provider may also monitor you closely for any potential complications, especially with long-term use. Additionally, do not stop using this medication abruptly without consulting your healthcare provider, as it may cause withdrawal symptoms or worsen your condition.

Additional Information:

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

Product Details:

**Composition:**Omeprazole for injection contains the active ingredient omeprazole, a proton pump inhibitor (PPI), at a strength of 40 mg per vial. It is typically supplied as a sterile lyophilized powder for reconstitution.
**Usage:**Omeprazole for injection is primarily used for the short-term treatment of conditions where oral therapy is not feasible or appropriate. These conditions may include:
1. **Gastroesophageal Reflux Disease (GERD)**: Omeprazole injection may be used for the management of severe GERD symptoms, such as erosive esophagitis, when oral medication is not an option or when rapid symptom relief is necessary.
2. **Peptic Ulcer Disease**: It can be used in cases of peptic ulcers, including duodenal and gastric ulcers, particularly when there is severe inflammation or bleeding.
3. **Zollinger-Ellison Syndrome**: Omeprazole injection is also indicated for the treatment of hypersecretory conditions such as Zollinger-Ellison syndrome, where there is excessive production of stomach acid.
**Administration:**The injection is typically given intravenously (IV) by a healthcare professional in a hospital or clinical setting. The dosage and duration of treatment depend on the specific condition being treated, the patient's medical history, and response to therapy.
**Side Effects:**While omeprazole for injection is generally well-tolerated, like all medications, it can cause side effects. Common side effects may include:
1. **Nausea and vomiting**: Some patients may experience mild gastrointestinal upset, including nausea or vomiting, particularly during the initial stages of treatment.
2. **Headache**: Headache is a relatively common side effect reported with the use of omeprazole.
3. **Diarrhea or constipation**: Changes in bowel habits, such as diarrhea or constipation, may occur, though these are usually mild and transient.
4. **Abdominal pain**: Some individuals may experience abdominal discomfort or pain.
5. **Dizziness**: Omeprazole may rarely cause dizziness or vertigo in some patients.
6. **Allergic reactions**: Although rare, allergic reactions such as rash, itching, swelling of the face, lips, or tongue, and difficulty breathing may occur. Seek immediate medical attention if any allergic reactions are experienced.
7. **Rare but serious side effects**: In rare cases, omeprazole may cause more serious adverse effects such as severe liver problems, pancreatitis, or low magnesium levels. 
It's essential to report any unusual or severe side effects to a healthcare professional promptly.
**Precautions:**- Omeprazole injection should be used with caution in patients with known hypersensitivity to omeprazole or other proton pump inhibitors.- Patients with liver or kidney impairment may require dosage adjustment or closer monitoring.- Omeprazole may interact with certain medications, so it's important to inform the healthcare provider about all medications being taken, including over-the-counter drugs and herbal supplements.
Always follow the prescribing physician's instructions and advice regarding the use of omeprazole injection, and do not hesitate to seek medical attention for any concerns or adverse reactions.

Additional Information:

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

Product Details:

**Composition:**Each vial of Pantoprazole for injection contains 40 mg of pantoprazole sodium as the active ingredient.
**Usage:**Pantoprazole for injection is primarily indicated for the short-term treatment of gastroesophageal reflux disease (GERD) in patients who are unable to take pantoprazole orally. It is also used for the treatment of pathological hypersecretory conditions like Zollinger-Ellison syndrome.
The injection is administered intravenously (IV) by a healthcare professional. The dosage and duration of treatment are determined by the severity of the condition and the individual patient's response to therapy.
**Side Effects:**While pantoprazole for injection is generally well-tolerated, some individuals may experience side effects. Common side effects include:
1. **Headache:** Mild to moderate headaches may occur during treatment with pantoprazole.2. **Nausea and Vomiting:** Some patients may experience nausea or vomiting as a side effect.3. **Abdominal Pain:** Abdominal discomfort or pain may occur, though this is usually mild.4. **Diarrhea or Constipation:** Changes in bowel habits, such as diarrhea or constipation, may occur in some individuals.5. **Dizziness:** Pantoprazole may cause dizziness or lightheadedness in some patients.6. **Injection Site Reactions:** Localized reactions at the injection site, such as pain, redness, or swelling, may occur.7. **Hypersensitivity Reactions:** Rarely, allergic reactions such as rash, itching, or swelling of the face, lips, or throat may occur. Severe allergic reactions (anaphylaxis) are extremely rare but require immediate medical attention.8. **Electrolyte Imbalance:** In rare cases, pantoprazole may cause imbalances in electrolytes, particularly magnesium. Symptoms of magnesium deficiency may include muscle spasms, irregular heartbeat, or seizures.
It's essential to inform your healthcare provider if you experience any side effects while receiving pantoprazole for injection. They can provide guidance on managing these side effects and may adjust your treatment regimen if necessary. Additionally, patients with certain medical conditions or those taking other medications should consult their healthcare provider before starting pantoprazole therapy to avoid potential drug interactions or complications.

Additional Information:

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

Product Details:

**Composition:**Rabeprazole Injection 20 mg contains the active ingredient rabeprazole, which is a proton pump inhibitor (PPI). Each vial typically contains 20 mg of rabeprazole sodium, along with suitable excipients to maintain stability and aid in administration.
**Usage:**Rabeprazole injection is primarily prescribed for the treatment of various acid-related gastrointestinal disorders, including:
1. **Gastric Ulcers:** Rabeprazole injection helps in healing and preventing the recurrence of gastric ulcers.2. **Duodenal Ulcers:** It aids in the healing and prevention of duodenal ulcers.3. **Gastroesophageal Reflux Disease (GERD):** Rabeprazole injection effectively manages symptoms associated with GERD such as heartburn, acid regurgitation, and difficulty swallowing.4. **Zollinger-Ellison Syndrome:** It is used in the management of Zollinger-Ellison Syndrome, a rare condition characterized by overproduction of stomach acid.5. **Erosive Esophagitis:** Rabeprazole injection helps in the healing of erosive esophagitis, a condition where the lining of the esophagus is damaged due to stomach acid.6. **Helicobacter pylori Eradication:** It is often used as part of a combination therapy to eradicate Helicobacter pylori bacteria, which can cause peptic ulcers.
Rabeprazole injection is typically administered intravenously by a healthcare professional in a hospital setting, especially in cases where oral administration is not feasible or advisable.
**Side Effects:**While rabeprazole injection is generally well-tolerated, like all medications, it may cause side effects in some individuals. Common side effects include:
1. **Headache:** Mild to moderate headaches are relatively common.2. **Nausea and Vomiting:** Some individuals may experience nausea or vomiting, especially when first starting the medication.3. **Abdominal Pain:** Mild abdominal discomfort or pain may occur.4. **Diarrhea or Constipation:** Changes in bowel habits such as diarrhea or constipation may occur.5. **Flatulence:** Increased gas production or bloating may occur in some individuals.6. **Dizziness:** Some people may experience dizziness or lightheadedness.7. **Fatigue:** Feelings of tiredness or fatigue may occur, although these are usually mild.8. **Rash:** Rarely, individuals may experience allergic reactions such as skin rash or itching.
It's essential to consult a healthcare professional if any side effects persist or worsen over time. Additionally, rare but severe side effects such as severe allergic reactions or liver problems may occur. If you experience any serious side effects, seek immediate medical attention.
It's important to inform your healthcare provider about any other medications or supplements you are taking before starting rabeprazole injection, as it may interact with certain drugs.

Additional Information:

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

Product Details:

Composition:Each vial contains Streptomycin Sulphate equivalent to 750 mg of Streptomycin.
Usage:Streptomycin Sulphate is an antibiotic used to treat various bacterial infections. It works by inhibiting the growth of bacteria. This medication is commonly prescribed for the treatment of tuberculosis, plague, tularemia, brucellosis, and certain other infections caused by susceptible strains of bacteria. Streptomycin is usually administered intramuscularly or intravenously under the supervision of a healthcare professional. The dosage and duration of treatment will be determined by the severity of the infection and the patient's response to the medication. It is important to complete the full course of treatment as prescribed by the healthcare provider, even if symptoms improve before the medication is finished.
Side Effects:Streptomycin Sulphate may cause some side effects, although not everyone will experience them. Common side effects include:
1. Nausea and vomiting2. Dizziness or lightheadedness3. Headache4. Injection site reactions, such as pain, swelling, or redness5. Diarrhea6. Ringing in the ears (tinnitus)7. Hearing loss (usually reversible but may be permanent with prolonged use or high doses)8. Kidney damage (especially with prolonged use or high doses)
It is important to inform your healthcare provider if you experience any side effects while taking Streptomycin Sulphate. In rare cases, this medication may cause serious allergic reactions or other severe side effects. If you experience symptoms such as difficulty breathing, rash, itching, swelling of the face, lips, or throat, or severe dizziness, seek immediate medical attention.
Note: This is not an exhaustive list of side effects. Please consult your healthcare provider or pharmacist for more information on potential side effects and precautions associated with Streptomycin Sulphate usage.

Additional Information:

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

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Composition:Teicoplanin is an antibiotic medication belonging to the glycopeptide class. Each vial of Teicoplanin injection typically contains 400 mg of teicoplanin powder for reconstitution. Teicoplanin works by inhibiting the synthesis of bacterial cell walls, thereby effectively treating bacterial infections.
Usage:Teicoplanin injection is primarily used for the treatment of severe bacterial infections caused by susceptible organisms. It is commonly employed in the management of infections such as:
1. Skin and soft tissue infections2. Bone and joint infections3. Endocarditis (infection of the heart's inner lining)4. Respiratory tract infections5. Bloodstream infections (bacteremia)6. Other serious bacterial infections caused by Gram-positive bacteria, including methicillin-resistant Staphylococcus aureus (MRSA)
Teicoplanin is usually administered intravenously (IV) or intramuscularly (IM). The dosage and duration of treatment depend on the severity of the infection, the patient's condition, and the susceptibility of the causative bacteria. It's essential to follow the prescribed dosage and complete the full course of treatment as directed by a healthcare professional, even if symptoms improve before the course is finished.
Side Effects:While Teicoplanin is generally well-tolerated, like any medication, it may cause adverse effects in some individuals. Common side effects may include:
1. Nausea and vomiting2. Diarrhea3. Rash or itching4. Pain or inflammation at the injection site (for IM administration)5. Headache6. Fever or chills7. Dizziness or lightheadedness8. Changes in kidney function, including elevated levels of creatinine9. Liver function abnormalities10. Allergic reactions, including severe skin reactions (Stevens-Johnson syndrome or toxic epidermal necrolysis) or anaphylaxis (rare)
It's crucial to inform your healthcare provider promptly if you experience any concerning symptoms while taking Teicoplanin. Additionally, patients with a history of hypersensitivity reactions to glycopeptide antibiotics should exercise caution and consult their healthcare provider before using Teicoplanin.
Note: This information serves as a general guideline. Always consult a healthcare professional for personalized medical advice and treatment recommendations.

Additional Information:

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

Product Details:

Composition:Each vial of Thiopental injection contains 500mg of thiopental sodium as the active ingredient. Other ingredients may include water for injection, sodium hydroxide or hydrochloric acid for pH adjustment, and possibly preservatives depending on the formulation.
Usage:Thiopental injection is a short-acting intravenous anesthetic agent primarily used for the induction of anesthesia prior to surgical procedures or other medical interventions requiring sedation. It acts quickly, typically within seconds to minutes after administration, and produces a rapid loss of consciousness.
Thiopental injection is administered intravenously by a healthcare professional in a hospital or clinical setting. The dosage and rate of administration depend on various factors including the patient's age, weight, medical condition, and the type of procedure being performed. It is important to follow the specific instructions provided by the healthcare provider.
Side Effects:Thiopental injection, like any medication, may cause side effects. Common side effects may include:
1. Respiratory depression: Thiopental can suppress breathing, leading to shallow or slowed breathing. This effect is more pronounced when higher doses are administered or when it is given rapidly.
2. Cardiovascular effects: Thiopental can cause changes in blood pressure and heart rate. It may lead to hypotension (low blood pressure) or bradycardia (slow heart rate).
3. Central nervous system effects: Thiopental may cause excitatory effects such as involuntary muscle movements, agitation, or delirium. It can also cause postoperative confusion or cognitive impairment.
4. Injection site reactions: Pain, irritation, or inflammation at the injection site may occur.
5. Allergic reactions: Rarely, individuals may experience allergic reactions such as itching, rash, or anaphylaxis (a severe allergic reaction).
6. Other effects: Nausea, vomiting, headache, dizziness, and drowsiness are possible side effects.
It is important for healthcare providers to monitor patients closely during and after administration of Thiopental injection to manage any potential side effects and ensure patient safety. Patients should inform their healthcare provider of any unusual or persistent side effects experienced during or after receiving Thiopental injection.

Additional Information:

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

Product Details:

**Composition:**Tigecycline for injection 50 mg is a sterile lyophilized powder for intravenous administration. Each vial contains tigecycline equivalent to 50 mg of tigecycline as the active ingredient.
**Usage:**Tigecycline is a broad-spectrum antibiotic used to treat various bacterial infections. It belongs to a class of antibiotics called glycylcyclines and works by inhibiting bacterial protein synthesis. Tigecycline is typically reserved for treating infections caused by multidrug-resistant bacteria or when other antibiotics have failed.
Dosage and administration:- Tigecycline is administered intravenously over a period of approximately 30 to 60 minutes.- The recommended dosage for adults is an initial dose of 100 mg followed by 50 mg every 12 hours.- The duration of treatment varies depending on the type and severity of the infection as well as the patient's response to therapy.- Tigecycline should not be mixed or co-administered with any other medications or solutions.
**Side Effects:**Like all medications, tigecycline can cause side effects. Common side effects include:1. Nausea and vomiting2. Diarrhea3. Headache4. Dizziness5. Changes in taste6. Injection site reactions (such as pain, redness, or swelling)7. Elevated liver enzymes8. Decreased appetite
Less common but more serious side effects may include:1. Severe allergic reactions (rash, itching, swelling of the face, tongue, or throat, difficulty breathing)2. Severe diarrhea (which may be a sign of a Clostridium difficile infection)3. Liver problems (signs may include yellowing of the skin or eyes, dark urine, abdominal pain)4. Pancreatitis (signs may include severe abdominal pain, nausea, vomiting)5. Increased intracranial pressure (signs may include severe headache, vision changes, confusion, seizures)
Patients should inform their healthcare provider if they experience any side effects while taking tigecycline. It's important to follow the prescribed dosage and duration of treatment to minimize the risk of side effects and ensure the effectiveness of the medication.

Additional Information:

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

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**Composition:**Vancomycin hydrochloride for injection typically contains 500 mg of vancomycin hydrochloride as the active ingredient. This medication is a glycopeptide antibiotic that is used to treat various bacterial infections.
**Usage:**Vancomycin hydrochloride for injection is administered intravenously and is typically used to treat severe infections caused by bacteria that are resistant to other antibiotics. It is commonly prescribed for infections such as:
1. Methicillin-resistant Staphylococcus aureus (MRSA) infections2. Clostridium difficile-associated diarrhea (CDAD)3. Endocarditis4. Bone infections5. Pneumonia6. Skin and soft tissue infections
It is essential to follow the dosage and administration instructions provided by the healthcare provider. The dosage may vary based on factors such as the severity of the infection, the patient's weight, and renal function. Vancomycin is usually administered slowly over at least 60 minutes to minimize the risk of adverse effects.
**Side Effects:**While vancomycin is an effective antibiotic, it can also cause certain side effects. Common side effects include:
1. Redness, swelling, or pain at the injection site2. Nausea and vomiting3. Diarrhea4. Kidney problems, including changes in urination frequency or volume5. Allergic reactions, such as rash, itching, or swelling of the face, lips, or tongue6. Low blood pressure7. Hearing loss (usually reversible and more common with higher doses or prolonged use)8. Blood disorders, such as thrombocytopenia or eosinophilia
It is important to inform the healthcare provider promptly if any side effects occur, especially if they persist or worsen over time. Additionally, patients should be monitored regularly for signs of adverse reactions, especially if they are receiving vancomycin for an extended period or have underlying health conditions.
In rare cases, vancomycin may cause severe adverse effects such as anaphylaxis, which requires immediate medical attention. Patients with a history of allergic reactions to vancomycin or other antibiotics should inform their healthcare provider before starting treatment.
Overall, while vancomycin is an essential antibiotic for treating serious bacterial infections, its use should be carefully monitored to minimize the risk of side effects and ensure effective treatment.

Additional Information:

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

Product Details:

Composition:Each vial of Voriconazole for injection contains 200 mg of voriconazole as the active ingredient.
Usage:Voriconazole for injection is primarily used in the treatment of serious fungal infections caused by Aspergillus spp., Candida spp., and certain other fungi in patients who have failed or are intolerant to other antifungal therapies. It is particularly indicated for invasive fungal infections in immunocompromised patients, such as those with neutropenia, hematopoietic stem cell transplant (HSCT) recipients, and those with invasive aspergillosis.
Dosage and administration should be determined by a healthcare professional based on the severity of the infection, the patient's weight, renal function, and other factors. The usual recommended dosage for adults is 6 mg/kg administered intravenously every 12 hours on the first day, followed by 4 mg/kg administered intravenously every 12 hours thereafter. For patients with mild to moderate hepatic impairment, a reduced dosage may be necessary.
Side Effects:Common side effects associated with voriconazole for injection include:
1. Visual disturbances (such as blurred vision, altered color perception, photophobia)2. Liver enzyme abnormalities3. Nausea and vomiting4. Rash5. Headache6. Fever7. Diarrhea8. Abnormalities in taste sensation9. Peripheral edema10. Abdominal pain
Serious side effects that may require immediate medical attention include severe liver dysfunction, severe allergic reactions (e.g., anaphylaxis), and cardiac arrhythmias. Patients should be monitored closely for signs of liver toxicity, including jaundice, abdominal pain, and abnormal liver function tests.
It's essential for patients to inform their healthcare provider about any new or worsening symptoms experienced during treatment with voriconazole for injection. Additionally, patients should be advised not to drive or operate machinery if they experience visual disturbances while using this medication.

Additional Information:

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

Product Details:

Composition:- Lincomycin Hydrochloride 600mg Injection
Usage:Lincomycin Hydrochloride is an antibiotic medication primarily used to treat various bacterial infections. It belongs to the class of antibiotics known as lincosamides. Lincomycin works by inhibiting bacterial protein synthesis, thereby preventing the growth and spread of bacteria.
This injection is typically prescribed for infections caused by susceptible strains of bacteria, including but not limited to:1. Skin and soft tissue infections2. Respiratory tract infections3. Bone and joint infections4. Intra-abdominal infections5. Septicemia6. Endocarditis7. Pelvic infections8. Other serious bacterial infections
Lincomycin Hydrochloride injection is administered intramuscularly or intravenously by a healthcare professional. The dosage and duration of treatment depend on the severity of the infection, the patient's condition, and other factors determined by the prescribing physician.
It's essential to complete the full course of treatment as prescribed, even if symptoms improve before completion. Stopping the medication prematurely can lead to the recurrence of the infection or the development of antibiotic-resistant bacteria.
Side Effects:While Lincomycin Hydrochloride is effective in treating bacterial infections, it may also cause some side effects. Common side effects may include:1. Nausea2. Vomiting3. Diarrhea4. Abdominal pain5. Injection site reactions (pain, swelling, or redness)6. Skin rash or itching7. Headache8. Dizziness9. Changes in taste
These side effects are usually mild and temporary. However, if any of these side effects persist or worsen, it's important to inform your healthcare provider promptly.
In rare cases, Lincomycin Hydrochloride may cause more severe side effects, including:1. Severe allergic reactions (difficulty breathing, swelling of the face, lips, tongue, or throat)2. Severe diarrhea or colitis (inflammation of the colon)3. Liver problems (yellowing of the skin or eyes, dark urine, abdominal pain)4. Blood disorders (unusual bleeding or bruising, persistent sore throat, fever)
If you experience any of these serious side effects, seek immediate medical attention.
It's crucial to inform your doctor about any pre-existing medical conditions, allergies, or other medications you're taking before starting Lincomycin Hydrochloride treatment to minimize the risk of adverse reactions or interactions.

Additional Information:

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

Product Details:

Composition:Amikacin 250mg Injection contains the active ingredient amikacin sulfate, which is a semi-synthetic aminoglycoside antibiotic. Each milliliter of the injection typically contains 250 milligrams of amikacin sulfate, along with suitable excipients and stabilizers.
Usage:Amikacin is primarily used to treat serious bacterial infections caused by susceptible organisms. It is often employed in cases where other antibiotics have failed or are not suitable due to resistance or allergies. Common uses include severe infections such as complicated urinary tract infections, respiratory tract infections, bloodstream infections, intra-abdominal infections, skin and soft tissue infections, bone and joint infections, and certain types of meningitis.
The dosage and duration of treatment with amikacin should be determined by a healthcare professional based on factors such as the severity of the infection, the patient's age, weight, renal function, and the susceptibility of the causative bacteria. It is typically administered via intramuscular or intravenous routes.
It is essential to follow the prescribed dosage regimen and complete the full course of treatment, even if symptoms improve before the medication is finished. Failure to do so may result in the recurrence of infection or the development of antibiotic resistance.
Side Effects:As with any medication, Amikacin Injection can cause side effects, although not everyone will experience them. Common side effects may include:
1. Nausea and vomiting2. Diarrhea3. Dizziness or lightheadedness4. Headache5. Injection site reactions such as pain, swelling, or irritation
More serious side effects are less common but may include:
1. Kidney damage or kidney failure, especially with prolonged use or high doses. Monitoring of renal function is typically recommended during treatment with amikacin.2. Hearing loss or tinnitus (ringing in the ears), which may be irreversible. This risk is higher with prolonged use, higher doses, or in patients with pre-existing hearing impairment.3. Neuromuscular blockade, leading to muscle weakness or paralysis, particularly in patients with myasthenia gravis or receiving neuromuscular-blocking agents.4. Allergic reactions, including rash, itching, swelling, or difficulty breathing. Anaphylaxis, while rare, is a severe allergic reaction that requires immediate medical attention.
Patients should report any unexpected or severe side effects to their healthcare provider promptly. It's crucial to weigh the potential benefits of treatment with Amikacin against the risks of adverse effects, and healthcare professionals will closely monitor patients receiving this medication.

Additional Information:

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

Product Details:

**Composition:**Chloroquine Phosphate 40mg Injection contains chloroquine phosphate as the active ingredient. Chloroquine phosphate is an antimalarial drug that works by interfering with the growth of parasites in the red blood cells of the human body.
**Usage:**Chloroquine Phosphate 40mg Injection is primarily used for the treatment and prevention of malaria caused by Plasmodium species. It may also be prescribed for certain autoimmune disorders, such as rheumatoid arthritis and lupus erythematosus.
- **Malaria Treatment:** The dosage regimen for malaria treatment typically involves an initial loading dose, followed by maintenance doses. The exact dosage and duration of treatment will be determined by the healthcare provider based on factors such as the severity of the infection, the patient's age, weight, and overall health.  - **Malaria Prevention:** Chloroquine Phosphate 40mg Injection may be used for malaria prophylaxis in individuals traveling to regions where malaria is endemic. It is usually started before entering the malaria-endemic area and continued during the stay and for a specific duration after leaving the area. The dosage and duration of prophylaxis will depend on factors such as the destination, duration of stay, and individual risk factors.
- **Autoimmune Disorders:** In the treatment of autoimmune disorders like rheumatoid arthritis and lupus erythematosus, Chloroquine Phosphate 40mg Injection may be prescribed as part of a comprehensive treatment plan. The dosage and duration of treatment will be determined by the healthcare provider based on the individual's condition and response to therapy.
**Side Effects:**While Chloroquine Phosphate 40mg Injection is generally well-tolerated, it may cause some side effects in certain individuals. Common side effects may include:
1. Gastrointestinal disturbances such as nausea, vomiting, diarrhea, or abdominal pain.2. Headache and dizziness.3. Visual disturbances, including blurred vision or changes in color vision.4. Skin reactions like itching, rash, or photosensitivity.5. Muscle weakness or loss of appetite.6. Blood disorders, including anemia or low platelet count.7. Cardiac effects such as QT interval prolongation or arrhythmias (rare).
It is essential to inform your healthcare provider if you experience any adverse reactions while using Chloroquine Phosphate 40mg Injection. Additionally, individuals with a history of certain medical conditions or those taking other medications should consult their healthcare provider before using this medication to prevent potential drug interactions or contraindications.
In rare cases, chloroquine phosphate may cause severe side effects, including retinopathy (damage to the retina), cardiomyopathy (heart muscle damage), or hypoglycemia (low blood sugar). Therefore, it is crucial to use this medication under the supervision of a healthcare professional and to undergo regular monitoring as recommended.

Additional Information:

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

Product Details:

Composition:Each mL of Paracetamol 750mg Injection contains 150mg of paracetamol (acetaminophen) as the active ingredient.
Usage:Paracetamol 750mg Injection is typically used for the management of moderate to severe pain when oral administration is not feasible or preferred, or when a rapid onset of action is required. It is commonly administered in hospital settings by healthcare professionals.
Indications for use may include:
1. Post-operative pain relief: After surgeries, especially those involving orthopedic procedures or abdominal surgeries.2. Management of acute pain: In conditions such as renal colic, severe musculoskeletal pain, or acute exacerbations of chronic pain syndromes.3. Fever: In cases where oral administration is not possible or when a rapid reduction in fever is required, such as in critically ill patients.
Dosage and Administration:The dosage and administration of Paracetamol 750mg Injection should be determined by a healthcare professional based on the patient's age, weight, medical condition, and response to treatment. The injection is typically administered intravenously (IV) or intramuscularly (IM). It should not be administered more frequently than every 4 to 6 hours, and the total daily dose should not exceed the recommended maximum to avoid the risk of hepatotoxicity.
Side Effects:While Paracetamol 750mg Injection is generally considered safe when used appropriately, it may cause side effects in some individuals. Common side effects may include:
1. Nausea and vomiting2. Injection site reactions (pain, redness, swelling)3. Hypotension (low blood pressure) or hypertension (high blood pressure)4. Liver toxicity or hepatic injury, especially with prolonged or excessive use
Rare but serious side effects may include:
1. Allergic reactions such as skin rash, itching, or hives2. Anaphylaxis (severe allergic reaction) - This is extremely rare but can be life-threatening and requires immediate medical attention.3. Blood disorders such as thrombocytopenia (low platelet count) or leukopenia (low white blood cell count)
It's essential to monitor patients closely for any signs of adverse reactions during and after administration. If any unusual or severe symptoms occur, medical attention should be sought immediately.
Precautions:1. Paracetamol 750mg Injection should be used with caution in patients with liver impairment or alcohol dependence.2. Avoid using other medications containing paracetamol concurrently to prevent exceeding the recommended maximum daily dose.3. Patients with a history of allergic reactions to paracetamol or other components of the injection should not use this medication.
Overall, Paracetamol 750mg Injection can be an effective option for pain relief and fever reduction when administered appropriately under medical supervision. However, careful monitoring and adherence to dosage guidelines are essential to minimize the risk of adverse effects. Always consult a healthcare professional for personalized advice regarding medication use.

Additional Information:

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

Product Details:

**Composition:**
Analgin 500 mg Injection contains the active ingredient Metamizole Sodium (also known as Dipyrone), which is a non-steroidal anti-inflammatory drug (NSAID) with analgesic (pain-relieving), antipyretic (fever-reducing), and anti-inflammatory properties.
**Usage:**
Analgin 500 mg Injection is typically used for the treatment of moderate to severe pain, fever, and inflammation. It is commonly prescribed for conditions such as:
1. Acute pain: Analgin can be used for pain relief in conditions like post-operative pain, renal colic, dental pain, etc.2. Fever: It is effective in reducing fever associated with various infections or inflammatory conditions.3. Inflammation: Analgin can help alleviate inflammation seen in conditions such as arthritis, sprains, and strains.
It is important to use Analgin Injection strictly as prescribed by a healthcare professional. The dosage and duration of treatment may vary depending on the individual's condition and medical history.
**Side Effects:**
While Analgin can be effective for pain relief and fever reduction, it may also cause certain side effects. Common side effects associated with Analgin 500 mg Injection include:
1. **Allergic reactions:** Some individuals may experience allergic reactions such as skin rash, itching, swelling of the face, lips, or tongue, difficulty breathing, etc. If any signs of allergic reaction occur, immediate medical attention is necessary.  2. **Gastrointestinal disturbances:** Analgin may cause gastrointestinal side effects such as nausea, vomiting, abdominal pain, or diarrhea.
3. **Blood disorders:** In rare cases, Analgin can lead to blood disorders such as agranulocytosis (a severe reduction in white blood cells), thrombocytopenia (low platelet count), or leukopenia (reduction in white blood cell count).
4. **Kidney and liver damage:** Prolonged use of Analgin or high doses may lead to kidney or liver damage. Individuals with pre-existing kidney or liver conditions should use Analgin with caution and under medical supervision.
5. **Decreased blood pressure:** Analgin may cause a drop in blood pressure, especially when administered rapidly through injection. This can lead to dizziness or fainting.
6. **Injection site reactions:** Pain, redness, or swelling at the injection site may occur.
It is essential to report any unusual or severe side effects to a healthcare professional promptly. Analgin should not be used without a prescription and should not be taken for an extended period without medical supervision. Individuals with certain medical conditions such as asthma, kidney or liver disease, or a history of blood disorders should use Analgin with caution and under medical guidance.

Additional Information:

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

Product Details:

**Composition:**Dexamethasone 4mg Injection typically contains Dexamethasone as the active ingredient. Dexamethasone is a synthetic corticosteroid that mimics the action of hormones produced by the adrenal glands. Each milliliter (mL) of the injection solution usually contains 4 milligrams (mg) of dexamethasone.
**Usage:**Dexamethasone 4mg Injection is used for various medical conditions where corticosteroid therapy is indicated. Some common uses include:
1. **Inflammatory Conditions:** It is used to reduce inflammation associated with conditions such as arthritis, asthma exacerbations, dermatitis, and allergic reactions.  2. **Immune System Disorders:** Dexamethasone is employed in the treatment of autoimmune diseases like lupus erythematosus and rheumatoid arthritis, where the immune system attacks healthy tissues.
3. **Allergic Reactions:** It is used to manage severe allergic reactions, including anaphylaxis, when other medications are ineffective.
4. **Certain Cancers:** Dexamethasone may be prescribed as part of chemotherapy protocols to reduce inflammation, swelling, and nausea associated with certain types of cancers, such as lymphoma and leukemia.
5. **Edema:** It can be used to reduce edema (fluid retention) associated with various conditions, such as brain tumors or cerebral edema.
6. **Endocrine Disorders:** In cases of adrenal insufficiency, dexamethasone can substitute for inadequate endogenous cortisol production.
**Side Effects:**Despite its therapeutic benefits, dexamethasone can cause several side effects, especially when used long-term or at high doses. Some common side effects include:
1. **Increased Appetite and Weight Gain:** Dexamethasone can stimulate appetite, leading to weight gain.
2. **Fluid Retention:** It may cause fluid retention, leading to swelling in various parts of the body, particularly in the face (moon face) and abdomen.
3. **Mood Changes:** Mood swings, irritability, anxiety, and even depression can occur with dexamethasone use.
4. **Insomnia:** Some individuals may experience difficulty falling asleep or staying asleep.
5. **Increased Blood Sugar Levels:** Dexamethasone can elevate blood glucose levels, posing a risk for individuals with diabetes or those predisposed to developing diabetes.
6. **Hypertension:** It can cause elevated blood pressure, which may require monitoring and management.
7. **Osteoporosis:** Long-term use of dexamethasone can weaken bones, leading to osteoporosis and an increased risk of fractures.
8. **Immune Suppression:** Dexamethasone suppresses the immune system, increasing the risk of infections and impairing wound healing.
9. **Gastrointestinal Effects:** It can cause stomach irritation, ulcers, and even gastrointestinal bleeding in some cases.
10. **Cataracts and Glaucoma:** Prolonged use of dexamethasone may increase the risk of developing cataracts and glaucoma.
11. **Adrenal Suppression:** Long-term use of dexamethasone can suppress the adrenal glands, leading to adrenal insufficiency when the medication is discontinued abruptly.
It is important for patients to be aware of these potential side effects and to discuss any concerns with their healthcare provider. Additionally, dexamethasone should not be stopped suddenly without medical supervision, as this can cause withdrawal symptoms and adrenal insufficiency.

Additional Information:

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

Product Details:

**Composition**:- **Active Ingredient**: Digoxin- **Strength**: 50 micrograms (mcg) per injection
**Usage**:- **Indications**: Digoxin is a medication primarily used to treat heart conditions such as heart failure and atrial fibrillation. It belongs to a class of drugs known as cardiac glycosides. The injection form of digoxin is typically reserved for situations where oral administration is not feasible or for patients who are unable to take medications by mouth.- **Administration**: Digoxin injection is usually administered intravenously (IV), either as a slow bolus injection or through a drip infusion. The dosage and rate of administration should be carefully determined by a healthcare professional based on the patient's condition and response to treatment. It is essential to follow proper injection techniques and dilution protocols to minimize the risk of adverse effects.- **Dosage**: The dosage of digoxin injection varies depending on factors such as the patient's age, weight, renal function, and the specific condition being treated. Dosage adjustments may be necessary based on regular monitoring of serum digoxin levels and clinical response.- **Monitoring**: Regular monitoring of cardiac function, electrolytes (especially potassium levels), and serum digoxin concentrations is crucial during digoxin therapy to prevent toxicity and ensure therapeutic efficacy.- **Duration of Treatment**: The duration of digoxin treatment is determined by the underlying condition being treated and the individual patient's response. It may be prescribed as a short-term or long-term therapy, often as part of a comprehensive management plan for heart failure or arrhythmias.
**Side Effects**:- **Common Side Effects**: Nausea, vomiting, loss of appetite, headache, dizziness, fatigue, visual disturbances (such as blurred or yellow-tinted vision), and various gastrointestinal symptoms are among the common side effects associated with digoxin use.- **Serious Side Effects**: Digoxin can cause serious adverse effects, particularly if the dosage is too high or if drug levels accumulate in the body. These may include severe arrhythmias (including ventricular tachycardia or fibrillation), heart block, electrolyte disturbances (especially hypokalemia), and toxicity-related manifestations such as confusion, delirium, and visual disturbances.- **Drug Interactions**: Digoxin interacts with numerous medications, including certain antibiotics, diuretics, calcium channel blockers, and antiarrhythmic drugs. Concurrent use of these medications may increase the risk of digoxin toxicity or alter its therapeutic effects. Healthcare professionals should carefully review the patient's medication regimen and consider potential drug interactions before prescribing digoxin.- **Contraindications**: Digoxin is contraindicated in patients with hypersensitivity to digoxin or other components of the formulation. It should be used with caution in patients with preexisting cardiac conditions, renal impairment, electrolyte imbalances, thyroid disorders, or hepatic dysfunction.
**Note**: The information provided here is for educational purposes only and should not substitute professional medical advice. Patients should always consult healthcare professionals for personalized guidance regarding medication use and potential side effects.

Additional Information:

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

Product Details:

**Composition:**Dimenhydrinate Hydrochloride 50mg Injection typically contains the active ingredient Dimenhydrinate Hydrochloride, which is a combination of diphenhydramine (an antihistamine) and 8-chlorotheophylline (a mild stimulant). Each milliliter of injection solution contains 50mg of Dimenhydrinate Hydrochloride.
**Usage:**Dimenhydrinate Hydrochloride Injection is commonly used in medical settings for the following purposes:
1. **Motion Sickness:** It is often administered to alleviate symptoms associated with motion sickness, such as nausea, vomiting, and dizziness.  2. **Nausea and Vomiting:** Dimenhydrinate Injection may also be used to manage nausea and vomiting caused by other factors, such as chemotherapy, surgery, or inner ear problems.
3. **Vertigo:** In cases of vertigo (a sensation of spinning or dizziness), Dimenhydrinate Injection can help relieve symptoms.
4. **Preoperative Sedation:** It may be used as a preoperative sedative to calm patients before surgery.
5. **Other Uses:** Dimenhydrinate Hydrochloride Injection may have off-label uses as determined by a healthcare professional.
**Side Effects:**While Dimenhydrinate Hydrochloride Injection is generally considered safe when used as directed by a healthcare provider, it may cause some side effects in certain individuals. Common side effects include:
1. **Drowsiness:** Dimenhydrinate is known to cause drowsiness and sedation, which may impair the ability to perform tasks that require alertness, such as driving or operating machinery.  2. **Dry Mouth:** Some individuals may experience a dry mouth sensation while using Dimenhydrinate Injection.
3. **Blurred Vision:** Blurred vision may occur as a side effect of Dimenhydrinate.
4. **Constipation:** Dimenhydrinate can sometimes lead to constipation.
5. **Urinary Retention:** In some cases, Dimenhydrinate may cause difficulty or inability to urinate.
6. **Dizziness:** While Dimenhydrinate is used to treat dizziness, paradoxically it may also cause dizziness as a side effect in some individuals.
7. **Allergic Reactions:** Rarely, allergic reactions such as skin rash, itching, swelling, or difficulty breathing may occur. If any of these symptoms occur, medical attention should be sought immediately.
It is important for patients to inform their healthcare provider about any side effects experienced while using Dimenhydrinate Hydrochloride Injection. Additionally, individuals with certain medical conditions or those taking other medications should consult with a healthcare professional before using this medication to avoid potential interactions or complications.

Additional Information:

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

Product Details:

**Composition:**
- **Active Ingredient:** Lidocaine 2% (20 mg/mL)- **Inactive Ingredients:** Typically, lidocaine injections contain other ingredients such as sodium chloride (for isotonicity), hydrochloric acid (for pH adjustment), and water for injection.
**Usage:**
*Lidocaine 2% Injection* is a local anesthetic solution used for various medical procedures and conditions where local numbing or anesthesia is required. It is administered by injection directly into the area needing anesthesia. Common uses include:
1. **Local Anesthesia:** Lidocaine 2% Injection is widely used for local anesthesia in various medical procedures, such as dental procedures, minor surgeries, and dermatological procedures.  2. **Pain Management:** It can be used for pain management in certain conditions like post-operative pain, neuropathic pain, and chronic pain syndromes.
3. **Arrhythmia Management:** In some cases, lidocaine injections are used for the management of certain types of cardiac arrhythmias.
4. **Nerve Blocks:** Lidocaine injections can be used for nerve blocks to provide regional anesthesia for surgeries or to manage chronic pain conditions.
5. **Emergency Situations:** It may also be used in emergency situations such as resuscitation procedures or during cardiac events.
The dosage and administration of lidocaine injection depend on the specific medical condition, the patient's age, weight, and overall health, and should be determined by a healthcare professional.
**Side Effects:**
While lidocaine injections are generally considered safe when used appropriately, they may cause certain side effects. Common side effects include:
1. **Local Reactions:** Pain, redness, swelling, or irritation at the injection site are common local reactions.
2. **Allergic Reactions:** Some individuals may experience allergic reactions to lidocaine, which can manifest as rash, itching, hives, or difficulty breathing. Severe allergic reactions such as anaphylaxis are rare but possible.
3. **Systemic Effects:** Lidocaine can sometimes cause systemic effects, especially if administered in large doses or if it enters the bloodstream inadvertently. These effects may include dizziness, lightheadedness, headache, blurred vision, tremors, nausea, vomiting, confusion, or seizures.
4. **Cardiovascular Effects:** In rare cases, lidocaine can affect the cardiovascular system, leading to changes in heart rate, blood pressure, or cardiac rhythm.
5. **Central Nervous System Effects:** Lidocaine can affect the central nervous system, causing symptoms such as drowsiness, confusion, or excitability.
It's essential to report any adverse reactions or side effects to a healthcare professional promptly. Lidocaine should be used cautiously in patients with a history of allergies, heart conditions, liver or kidney disease, or neurological disorders. Pregnant or breastfeeding women should also consult with their healthcare provider before using lidocaine injections.

Additional Information:

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

Product Details:

Composition:- Lidocaine 2% (20 mg/mL)- Adrenaline (Epinephrine) 0.1 mg/mL
Usage:This injection is typically utilized as a local anesthetic with vasoconstrictive properties. It is commonly employed in various medical procedures, including but not limited to:1. Dental procedures: for local anesthesia during tooth extraction, root canal treatment, etc.2. Minor surgical procedures: for numbing the skin and underlying tissues before incisions or suturing.3. Regional anesthesia: for nerve blocks, epidural anesthesia, etc.4. Emergency medicine: for wound closure, foreign body removal, etc.5. Diagnostic procedures: for numbing the skin before biopsy, lumbar puncture, etc.
Dosage and administration should be determined by a qualified healthcare professional based on the patient's condition, the specific procedure, and individual factors such as age and weight. It is typically administered via injection directly into the targeted area.
Side Effects:While lidocaine with adrenaline is generally considered safe when used appropriately, it may cause some side effects in certain individuals. Common side effects may include:1. Local reactions at the injection site such as pain, swelling, redness, or bruising.2. Nausea or vomiting.3. Dizziness or lightheadedness.4. Headache.5. Increased heart rate or palpitations due to the adrenaline component.6. High blood pressure.7. Anxiety or restlessness.8. Allergic reactions, although rare, which may manifest as rash, itching, difficulty breathing, or swelling of the face, lips, tongue, or throat.
It's crucial to report any unexpected or severe side effects to a healthcare provider promptly. Additionally, patients with a known allergy to lidocaine, adrenaline, or any component of the injection should avoid its use and inform their healthcare provider immediately.

Additional Information:

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

Product Details:

**Composition:**- Active ingredient: Magnesium sulfate heptahydrate 0.2% (w/v)- Inactive ingredients: Sterile water for injection
**Usage:**Magnesium sulfate injection is used for various medical purposes, including:1. **Magnesium Deficiency:** It is administered intravenously to correct magnesium deficiency.2. **Pre-eclampsia/Eclampsia:** In obstetrics, it is often used to prevent seizures in women with pre-eclampsia or eclampsia during pregnancy.3. **Torsades de Pointes:** It may be used to treat certain types of irregular heartbeat (arrhythmias), such as torsades de pointes.4. **Asthma:** In some cases, it may be used as an adjunct treatment for severe acute asthma.5. **Constipation:** Occasionally, it is used as a laxative in certain situations, although this is less common.
**Dosage and Administration:**Dosage and administration should be determined by a qualified healthcare professional based on the patient's condition, age, weight, and other factors. It is usually administered intravenously under medical supervision.
**Side Effects:**1. **Flushing and sweating:** Some individuals may experience flushing and sweating due to the vasodilatory effects of magnesium sulfate.2. **Hypotension:** Intravenous administration of magnesium sulfate can cause a drop in blood pressure, leading to hypotension.3. **Respiratory depression:** In high doses, magnesium sulfate can suppress respiratory function, leading to respiratory depression.4. **Muscle weakness:** Excessive magnesium levels can cause muscle weakness or paralysis.5. **Cardiac arrest:** Rarely, excessively high levels of magnesium sulfate can lead to cardiac arrest.6. **Allergic reactions:** Some individuals may experience allergic reactions to magnesium sulfate injection, such as rash, itching, or swelling.
**Note:** This is not an exhaustive list of side effects. Patients should be monitored closely during administration, and any unusual symptoms should be reported to a healthcare professional immediately. Magnesium sulfate should only be administered under the supervision of a qualified healthcare provider.

Additional Information:

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

Product Details:

**Composition:**Methylprednisolone acetate 20mg injection contains the active ingredient methylprednisolone, which is a synthetic glucocorticoid. Each milliliter of the injection typically contains 20 milligrams of methylprednisolone acetate as the active ingredient along with inactive ingredients necessary for the formulation.
**Usage:**Methylprednisolone acetate 20mg injection is primarily used for its potent anti-inflammatory and immunosuppressive properties. It is administered via injection, usually intramuscularly or intra-articularly, under the supervision of a healthcare professional. Here are some common uses:
1. **Inflammatory Conditions:** It is indicated for the treatment of various inflammatory conditions such as arthritis, bursitis, tendonitis, synovitis, and other joint disorders where inflammation is a primary component.   2. **Allergic Reactions:** Methylprednisolone acetate injection may be prescribed for the management of severe allergic reactions, including anaphylaxis, when oral or intravenous administration is not feasible.
3. **Autoimmune Diseases:** In autoimmune diseases such as systemic lupus erythematosus (SLE) or rheumatoid arthritis (RA), methylprednisolone acetate injection may be used as part of a treatment regimen to suppress the immune response and reduce inflammation.
4. **Dermatological Conditions:** It can also be used for certain dermatological conditions like severe eczema or psoriasis when other treatments have failed.
5. **Respiratory Disorders:** In some cases, it may be used as an adjunctive therapy for severe asthma exacerbations or chronic obstructive pulmonary disease (COPD) exacerbations.
It's important to note that the dosage and duration of treatment with methylprednisolone acetate injection should be determined by a healthcare professional based on the specific condition being treated and the individual patient's response to treatment.
**Side Effects:**Like any medication, methylprednisolone acetate injection can cause side effects, although not everyone will experience them. Some common side effects include:
1. **Gastrointestinal Disturbances:** These may include stomach irritation, nausea, vomiting, or abdominal pain.
2. **Fluid Retention:** Edema or fluid retention may occur, leading to swelling of the extremities or weight gain.
3. **Increased Appetite:** Some individuals may experience an increase in appetite, which can lead to weight gain.
4. **Mood Changes:** Methylprednisolone acetate injection can affect mood, leading to mood swings, irritability, or anxiety.
5. **Insomnia:** Difficulty sleeping or insomnia may occur, especially when the medication is taken later in the day.
6. **Hyperglycemia:** Methylprednisolone can increase blood glucose levels, particularly in individuals with diabetes or those predisposed to developing diabetes.
7. **Immunosuppression:** Prolonged use of methylprednisolone acetate injection can suppress the immune system, increasing the risk of infections.
8. **Osteoporosis:** Long-term use of corticosteroids like methylprednisolone can weaken bones, leading to osteoporosis and an increased risk of fractures.
9. **Adrenal Suppression:** Prolonged use of methylprednisolone acetate injection can suppress the function of the adrenal glands, which produce natural corticosteroids, leading to adrenal insufficiency when the medication is discontinued abruptly.
10. **Skin Changes:** Some individuals may experience thinning of the skin, easy bruising, or delayed wound healing.
It's essential to discuss any concerns or potential side effects with a healthcare professional before starting treatment with methylprednisolone acetate injection. Additionally, abrupt discontinuation of the medication should be avoided, and the dosage should be tapered gradually under medical supervision to prevent withdrawal symptoms and adrenal insufficiency.

Additional Information:

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

Product Details:

**Composition:**
Methylcobalamin 0.50mg Injection typically contains the following active ingredient:
- Methylcobalamin: 0.50mg
**Usage:**
Methylcobalamin is a form of vitamin B12, which is essential for various bodily functions including the maintenance of nerve cells, red blood cells, and DNA synthesis. Methylcobalamin injection is commonly used to treat vitamin B12 deficiency, particularly in cases where oral supplementation is not effective or feasible. It is also used in the treatment of certain neurological conditions such as peripheral neuropathy, diabetic neuropathy, and other nerve-related disorders.
The injection is administered intramuscularly by a healthcare professional, typically into the upper arm or buttock, as directed by a doctor. Dosage and frequency of administration vary depending on the severity of the deficiency and the individual's response to treatment. It is important to follow the dosage instructions provided by the healthcare provider.
**Side Effects:**
While Methylcobalamin injection is generally well-tolerated, some individuals may experience side effects. Common side effects may include:
1. Injection site reactions such as pain, redness, or swelling.2. Nausea or vomiting.3. Headache.4. Dizziness.5. Allergic reactions such as rash, itching, or difficulty breathing (rare but serious).
It is important to seek medical attention if any side effects persist or worsen over time. Additionally, inform your healthcare provider immediately if you experience any signs of an allergic reaction.
This list may not include all possible side effects. If you notice any other effects not listed above, contact your doctor or pharmacist for advice.
Note: This information is for informational purposes only and should not be considered as medical advice. Always consult a healthcare professional for proper diagnosis and treatment.

Additional Information:

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