Fibanix 12.5 mg/250 ml is a iv infusion manufactured by Beacon Pharmaceuticals PLC in Bangladesh. Its active ingredient is Tirofiban Hydrochloride.

Indications

Fibanix is indicated to reduce the rate of thrombotic cardiovascular events (combined endpoint of death, myocardial infarction, or refractory ischemia/repeat cardiac procedure) in patients with non-ST elevation acute coronary syndrome (NSTE-ACS).

Contraindications

Tirofiban Hydrochloride is contraindicated in patients with:
Severe hypersensitivity reaction to AGGRASTAT (i.e., anaphylactic reactions).
A history of thrombocytopenia following prior exposure to AGGRASTAT.
Active internal bleeding or a history of bleeding diathesis, major surgical procedure or severe physical trauma within the previous month.

Pharmacology

Tirofiban is a reversible antagonist of fibrinogen binding to the GP IIb/IIIa receptor, the major platelet surface receptor involved in platelet aggregation. When administered intravenously, Tirofiban inhibits ex vivo platelet aggregation in a dose- and concentration-dependent manner. When given according to the PRISM-PLUS regimen of 0.4 mcg/kg/min over 30 minutes followed by a 0.1 mcg/kg/min maintenance infusion, >90% inhibition of platelet aggregation is attained by the end of the 30-minute infusion. When given according to the recommended regimen of 25 mcg/kg followed by a 0.15 mcg/kg/min maintenance infusion, >90% inhibition of platelet aggregation is attained within 10 minutes. Platelet aggregation inhibition is reversible following cessation of the infusion of Tirofiban.

Dosage & Administration

Administer intravenously 25 mcg/kg within 5 minutes and then 0.15 mcg/kg/min (or 0.075 mcg/kg/min for patients with serum creatinine ≤60 mL/min), for up to 18 hours.

Pediatric Use: Safety and effectiveness in pediatric patients have not been established

Important Administration Instructions

To open the container, first tear off its foil overpouch. The plastic may be somewhat opaque because of moisture absorption during sterilization; the opacity will diminish gradually. Check for leaks by squeezing the inner bag firmly; if any leaks are found or sterility is suspect then the solution should be discarded. Do not use unless the solution is clear and the seal is intact. Suspend the container from its eyelet support, remove the plastic protector from the outlet port, and attach a conventional administration set.

You may administer AGGRASTAT in the same intravenous line as atropine sulfate, dobutamine, dopamine, epinephrine hydrochloride (HCl), famotidine injection, furosemide, lidocaine, midazolam HCl, morphine sulfate, nitroglycerin, potassium chloride, and propranolol HCl. Do not administer AGGRASTAT through the same IV line as diazepam.

Do not add other drugs or remove solution directly from the bag with a syringe.

Do not use plastic containers in series connections; such use can result in air embolism by drawing air from the first container if it is empty of solution.

Discard any unused portion left in the bag.

Interaction

Coadministration of antiplatelet agents, thrombolytics, heparin, or aspirin increases the risk of bleeding.

Side Effects

Bleeding is the most commonly reported adverse reaction.

Pregnancy & Lactation

Pregnancy Category B. There are no adequate and well-controlled studies in pregnant women. Tirofiban has been shown to cross the placenta in pregnant rats and rabbits. Studies with tirofiban HCl at intravenous doses up to 5 mg/kg/day (about 5 and 13 times the maximum recommended daily human dose for rat and rabbit, respectively, when compared on a body surface area basis) have revealed no harm to the fetus.

Nursing Mothers: It is not known whether tirofiban is excreted in human milk. However, significant levels of tirofiban were shown to be present in rat milk. Because many drugs are excreted in human milk, and because of the potential for adverse effects on the nursing infant, discontinue nursing or discontinue AGGRASTAT.

Precautions & Warnings

General Risk of Bleeding

: Bleeding is the most common complication encountered during therapy with Fibanix. Most bleeding associated with Fibanix occurs at the arterial access site for cardiac catheterization. Minimize the use of traumatic or potentially traumatic procedures such as arterial and venous punctures, intramuscular injections, nasotracheal intubation, etc. Concomitant use of fibrinolytics, oral anticoagulants and antiplatelet drugs increases the risk of bleeding.

Thrombocytopenia

: Profound thrombocytopenia has been reported with Fibanix. Monitor platelet counts beginning about 6 hours after treatment initiation and daily thereafter. If the platelet count decreases to <90,000/mm3, monitor platelet counts to exclude pseudothrombocytopenia. If thrombocytopenia is confirmed, discontinue Fibanix and heparin. Previous exposure to a glycoprotein (GP) IIb/IIIa receptor antagonist may increase the risk of developing thrombocytopenia.

Storage Conditions

Store at 25°C with excursions permitted between 15-30°C. Do not freeze. Protect from light during storage.

Disclaimer: This information is for reference only. Always consult a registered physician before taking any medicine.

Tirofiban Hydrochloride — all brand prices