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Tufehart 500mg Injection

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Prescription Required

Marketer

Alembic Pharmaceuticals Ltd

Salt Composition

Ferric Carboxymaltose (50mg/ml)

Overview Tufehart 500mg Injection

Ferrous-replacement injection, Tufehart 500mg, combats iron-deficiency anemia—a condition marked by low red blood cell counts due to insufficient iron. Red blood cell production, vital for oxygen transport, relies on iron. Administered intravenously by a healthcare professional via injection or infusion, Tufehart 500mg is typically given in two doses, a week apart, with careful monitoring for allergic reactions. Dosage frequency is determined by your physician based on your anemia's severity. A balanced diet rich in iron (found in foods like meat, eggs, dried fruit, leafy greens, and legumes) complements treatment. Common, generally transient side effects include nausea, headache, vertigo, elevated blood pressure, and injection site discomfort. Persistent or bothersome side effects warrant medical attention. This medication is contraindicated for non-iron deficiency anemias. Prior to treatment, disclose any conditions such as rheumatoid arthritis, respiratory allergies, hypertension, or liver disease, as these may influence treatment. Consult your doctor regarding use during pregnancy or breastfeeding. Regular blood tests will assess your iron levels, monitor treatment efficacy, and detect side effects. Limiting alcohol consumption during treatment is recommended.

Uses of Tufehart 500mg Injection

Managing iron-deficiency anemia

Major Benefits of Tufehart 500mg Injection:

This medication will be administered by your healthcare provider. Self-medication is strictly prohibited.

Common Side effects of Tufehart 500mg Injection:

  • Headache
  • Dizziness
  • High blood pressure
  • Injection site reactions (pain, swelling, redness)
  • Vomiting
  • Nausea
  • Dark colored stool

How to use Tufehart 500mg Injection:

This medication will be administered by your healthcare provider. Self-medication is strictly prohibited.

How Tufehart 500mg Injection works:

Ferrous sulfate injection, 500mg strength, treats iron deficiency anemia. This medication restores depleted iron levels, crucial for red blood cell production and hemoglobin synthesis—the oxygen-carrying component of red blood cells.

SAFETY ADVICE

AlcoholAlcoholCONSULT YOUR DOCTOR

Alcohol consumption alongside Tufehart 500mg Injection may pose unknown risks. Seek medical advice before combining them.

PregnancyPregnancyCONSULT YOUR DOCTOR

Administering Tufehart 500mg Injection during pregnancy may pose risks. While human data is scarce, animal research indicates potential harm to the fetus. A physician will assess the advantages against possible hazards prior to prescribing. Seek medical advice.

Breast feedingBreast feedingSAFE IF PRESCRIBED

Lactation is compatible with the use of Tufehart 500mg Injection. Research in humans indicates negligible transfer of the medication into breast milk, posing no identified risk to the infant.

DrivingDrivingSAFE

Driving ability is typically unaffected by a 500mg Tufehart injection.

KidneyKidneySAFE IF PRESCRIBED

The use of Tufehart 500mg Injection in individuals with impaired kidney function appears to present a low risk. Existing evidence indicates dose modification for Tufehart 500mg Injection might be unnecessary in such cases. However, medical advice should be sought.

LiverLiverCAUTION

Caution is advised when administering Tufehart 500mg Injection to individuals with hepatic impairment; dosage modification may be necessary. Physician consultation is recommended.

What if you forget to take Tufehart 500mg Injection :

Omit a scheduled Tufehart 500mg Injection? Seek medical advice immediately.

Facts to Know About Tufehart 500mg Injection

LabelValue
Type of Compound Iron-carbohydrate compound
Addictive None.
Medication Category Women's health

FAQs on Tufehart 500mg Injection

Trained personnel experienced in managing severe allergic responses (anaphylaxis) must administer Tufehart 500mg Injection. This injection may be given undiluted intravenously, or via a dialysis machine if applicable. Alternatively, it can be diluted with saline solution and infused intravenously. Post-injection observation of the patient should continue for at least 30 minutes. Subcutaneous or intramuscular administration is contraindicated.
Store Tufehart 500mg injection vials between 20°C and 25°C (68°F and 77°F). Freezing must be avoided. Acceptable temperature fluctuation is limited to a range of 15°C to 30°C (59°F to 86°F).
This medication is typically administered in two injections, spaced one week apart. Hemoglobin levels are subsequently evaluated no sooner than four weeks post-final injection to permit sufficient red blood cell regeneration. Further treatment may be considered based on individual iron levels if deficiency persists.
Tufehart 500mg Injection can temporarily elevate blood pressure, potentially causing facial flushing, dizziness, and nausea. These side effects may appear soon after administration and typically resolve within half an hour.
Improper injection of Tufehart 500mg can result in medication leakage at the injection site. Leakage necessitates immediate cessation of administration. Such leakage may induce skin irritation and persistent brown skin discoloration at the injection site.
Insufficient information exists regarding the administration of Tufehart 500mg Injection to pregnant individuals. Disclosing your pregnancy or pregnancy plans to your physician is crucial. Should pregnancy occur while using Tufehart 500mg Injection, seek immediate medical counsel. Your doctor will determine the appropriate course of action, potentially continuing or ceasing treatment.
Tufehart 500mg Injection
1,559
MRP 1,899
17% off