FREHEMGO® has a proven safety profile1–5
FREHEMGO® has a proven safety profile with no safety concerns reported, and almost no injection pain.*,**1–5 FPO
No thromboembolic events
No events reported, including no arterial or venous thrombotic events, or thrombotic microangiopathies1–5
No disruption for surgery
No surgeries or procedures required discontinuation of FREHEMGO®1–5
No neutralising antibodies
No clinical evidence of neutralising antibodies1–5
FREHEMGO® was well tolerated across clinical trials1
Pooled safety data from 448 participants across three Phase III clinical studies1
| Adverse drug reaction (ADR) | Number of patients (N=448) n (%) |
|---|---|
| Injection site reaction (ISR)* | 54 (12.1%) |
| Prothrombin fragment 1.2 increased | 43 (9.6%)verify — source PPT reads 4.3 |
| Fibrin D-dimer increased | 9 (2.0%) |
The safety profile was similar between children, adolescents, and adult participants FPO
The AE table / ISR information from screen 4.2 of the eCVA will also be presented here. FPO
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FPONormal levels all month long
Learn how FREHEMGO® normalises thrombin generation all month long.
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FPOThe freedom of zero bleeds
Discover powerful protection at every stage of the hemophilia journey.
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FPODosing made simple
No mg/kg dosing. No dose calculations — 5 prefilled pens.
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