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Brand Name :
Fraxiparine, Fraxiparine Forte
Synonyms :
nadroparin
Class :
Anticoagulant, Anticoagulant, Low Molecular Weight Heparin
Dosage Forms & StrengthsÂ
Solution Prefilled SyringeÂ
2850 units/0.3 mlÂ
15200 units/0.8 mlÂ
9500 units/mlÂ
11400 units/0.6 mlÂ
3800 units/0.4 mlÂ
5700 units/0.6 mlÂ
19000 units/mlÂ
Administer initial dose of 86 anti-Xa units/kg intravenously once bolus and the maximum dose not more than 9500 anti-Xa units
Fixed dosing:
<50 kg: dose of 3800 anti-Xa units once intravenous bolus
≥100 kg: dose of 9500 anti-Xa units once intravenous bolus
Administer maintenance dose of 86 anti-Xa units/kg subcutaneously each 12 hours and the maximum total daily dose not more than 19000 anti-Xa units
Fixed dosing:
<50 kg: dose of 3800 anti-Xa units subcutaneously each 12 hours
≥100 kg: dose of 9500 anti-Xa units subcutaneously each 12 hours
For Patients with standard bleeding risk:
Administer dose of 171 anti-Xa units/kg subcutaneously one time a day
Fixed dosing:
40 to 49 kg: dose of 7600 anti-Xa units subcutaneously one time daily
≥90 kg: dose of 17100 anti-Xa units subcutaneously one time daily
For Patients with increased risk for bleeding:
Administer dose of 86 anti-Xa units/kg subcutaneously each 12 hours
Fixed dosing:
40 to 49 kg: dose of 3800 anti-Xa units subcutaneously each 12 hours
≥90 kg: dose of 8550 anti-Xa units subcutaneously each 12 hours
Safety and efficacy not determined Â
Refer to adult dosingÂ
When nadroparin is used together with sertraline, the risk or seriousness of bleeding may be enhanced
when used with nadroparin, andexanet alfa's therapeutic efficacy may be lowered
Actions and SpectrumÂ
nadroparin works by inhibiting the activity of certain clotting factors in the blood, particularly factor Xa and thrombin. Â
By inhibiting them, nadroparin helps to prevent the formation of new blood clots and stabilizes existing clots.
Frequency not defined Â
Venous thrombosisÂ
Skin necrosisÂ
CalcinosisÂ
Arterial thrombosisÂ
Thromboembolism Â
Hypoaldosteronism Â
PriapismÂ
EosinophiliaÂ
Increased serum alanine aminotransferaseÂ
HemorrhageÂ
ThrombocythemiaÂ
ThrombocytopeniaÂ
Increased serum aspartate aminotransferaseÂ
Angioedema, hypersensitivity reactionÂ
Nonimmune anaphylaxisÂ
Injection site reactionÂ
OsteopeniaÂ
Post marketing report Â
Skin rashÂ
Urticaria Â
Pruritus Â
Erythema of skinÂ
HeadacheÂ
MigraineÂ
Black Box WarningÂ
None
Contraindication/Caution:Â
Contraindication:Â
Caution:Â
Pregnancy consideration:Â
Pregnancy category: N/AÂ
Lactation: Excretion into human milk is unknown Â
Pregnancy Categories:        Â
Category A: well-controlled and Satisfactory studies show no risk to the fetus in the first or later trimester.Â
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 category.Â
Pharmacology Â
nadroparin binds to antithrombin III (AT III), a natural anticoagulant in the body, and enhances its inhibitory effect on Factor Xa and thrombin. Â
PharmacodynamicsÂ
nadroparin’s inhibition of thrombin helps stabilize existing blood clots and prevents them from growing.Â
nadroparin has a mild inhibitory effect on platelet activation, which further contributes to its anticoagulant action.Â
PharmacokineticsÂ
Absorption  Â
nadroparin is absorbed into the bloodstream from the subcutaneous tissue. Â
DistributionÂ
nadroparin circulates throughout the body, distributing to various tissues and organs.Â
MetabolismÂ
nadroparin is not significantly metabolized by the body. Its primary mode of action is to bind to antithrombin III (ATIII) to exert its anticoagulant effect.Â
Elimination and excretionÂ
The elimination of nadroparin primarily occurs through renal clearance.
AdministrationÂ
nadroparin is a medication that is administered through subcutaneous injection. Â
It available in the form of pre-filled syringes with a needle for injection.
Patient information leafletÂ
Generic Name: nadroparinÂ
Why do we use nadroparin?Â
nadroparin is used to prevent deep vein thrombosis, which is the formation of blood clots in the deep veins. Â
nadroparin is used as a preventive measure to reduce the risk of pulmonary embolism in high-risk patients.  Â
nadroparin is used as an anticoagulant during hemodialysis procedures to prevent clotting in the dialysis. Â