Anthropometric Measurements as Predictors of Low Birth Weight Among Tanzanian Neonates: A Hospital-Based Study
November 7, 2025
Brand Name :
Fluxum
Synonyms :
parnaparin
Class :
Anti-coagulant,Thrombolytic
Dosage Forms & StrengthsÂ
Solution for injectionÂ
3200 unitsÂ
Indicated for Preoperative venous thromboembolism prevention:
For Surgical General Procedures: As sodium- Inject 3200 units 2 hours before the surgery subcutaneously, then 3200 units once daily for seven days, or until a patient is entirely ambulant.
For Orthopaedic patients or High-risk surgery: Inject 4250 units 12 hours before the operation, 4250 units 12 hours after the procedure subcutaneously, and after that once daily for 10 days.
Thromboembolic disorders
As sodium: Administer Injection of 6400 units for 7 to 10 days.
Safety and efficacy not establishedÂ
Refer adult dosingÂ
may increase the risk of haemorrhage with oral anticoagulants
may increase the risk of haemorrhage with oral anticoagulants
may increase the risk of haemorrhage with oral anticoagulants
may increase the risk of haemorrhage with oral anticoagulants
may increase the risk of haemorrhage with oral anticoagulants
parnaparin: it may decrease the therapeutic efficacy of soyabean oil
Actions and Spectrum:Â
parnaparin, like other LMWHs, works primarily by enhancing the activity of antithrombin III, a natural anticoagulant protein in the body. Antithrombin III inactivates several clotting factors, including thrombin (factor IIa) and factor Xa, essential components in the coagulation cascade that leads to blood clot formation.Â
LMWHs have a higher affinity for factor Xa compared to thrombin. parnaparin, being an LMWH, predominantly inhibits factor Xa. By binding to antithrombin III and accelerating its interaction with factor Xa, parnaparin inhibits the conversion of prothrombin to thrombin and reduces the formation of fibrin clots.Â
The spectrum of activity of parnaparin primarily involves its anticoagulant effects. It’s used for various clinical indications where anticoagulation is required. These indications can include:Â
Frequency not definedÂ
Injection site reactionÂ
BleedingÂ
Black box warning:Â
NoneÂ
Contraindications/caution:Â
Contraindications:Â
Pregnancy consideration: N/AÂ
Lactation: N/AÂ
Pregnancy category:Â
Category A: well-controlled and Satisfactory studies show no risk to the fetus in the first or later trimester.Â
<b>Category B: there was no evidence of risk to the fetus in animal studies, and there were not enough studies on pregnant women.Â
Category C: there was evidence of risk of adverse effects in animal reproduction studies, and no adequate evidence in human studies must take care of potential risks in pregnant women.   Â
Category D: adequate data with sufficient evidence of human fetal risk from various platforms, but despite the potential risk, and used only in emergency cases for potential benefits.   Â
Category X: Drugs listed in this category outweigh the risks over benefits. Hence these categories of drugs need to be avoided by pregnant women.   Â
Category N: There is no data available for the drug under this categoryÂ
Pharmacology:Â
parnaparin works primarily by enhancing the activity of antithrombin III (ATI), a natural anticoagulant protein in the body. It binds to ATIII and accelerates its inactivation of several clotting factors, particularly factor Xa and, to a lesser extent, thrombin (factor IIa). The inhibition of factor Xa interrupts the coagulation cascade and reduces the conversion of prothrombin to thrombin, thus preventing the formation of fibrin clots.Â
Pharmacokinetics:Â
AbsorptionÂ
parnaparin is administered through subcutaneous injection. Upon injection, it is absorbed into the bloodstream from the injection site. Subcutaneous administration allows for a gradual and controlled release of the medication into the systemic circulation.Â
DistributionÂ
parnaparin primarily distributed within the blood. As an anticoagulant, it must interact with clotting factors in the bloodstream to exert its effects. Parnaparin is designed to have a higher affinity for factor Xa, a key component in the coagulation cascade.Â
MetabolismÂ
parnaparin undergoes both renal and hepatic metabolism. Some of the medication is metabolized by the kidneys and the liver, leading to the breakdown of its components. The metabolism of Parnaparin contributes to its elimination from the body.Â
Elimination and ExcretionÂ
parnaparin is primarily excreted via the urine. The kidneys play a crucial role in eliminating the medication and its metabolites from the body. The excretion of Parnaparin through the urine removes it from the bloodstream, which helps maintain proper coagulation balance.Â
Administration:Â
It is administered through subcutaneous injection.Â
Patient information leafletÂ
Generic Name: parnaparinÂ
Why do we use parnaparin?Â
parnaparin is a low molecular weight heparin (LMWH) used for various medical conditions requiring anticoagulation. Its main uses include:Â