FIBRINOGEN HUMAN for Hypofibrinogenaemia: Side Effects & Safety Data
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There are 41 adverse event reports in the FDA FAERS database where FIBRINOGEN HUMAN was used for Hypofibrinogenaemia.
Most Reported Side Effects for FIBRINOGEN HUMAN
| Side Effect | Reports | % | Deaths | Hosp. |
|---|---|---|---|---|
| Foetal exposure during pregnancy | 40 | 9.8% | 0 | 26 |
| No adverse event | 38 | 9.3% | 3 | 9 |
| Off label use | 38 | 9.3% | 7 | 10 |
| Drug ineffective | 34 | 8.3% | 11 | 11 |
| Hypotension | 31 | 7.6% | 0 | 4 |
| Foetal anaemia | 27 | 6.6% | 0 | 27 |
| Foetal growth restriction | 27 | 6.6% | 0 | 27 |
| Haemorrhage in pregnancy | 26 | 6.4% | 0 | 26 |
| Anaphylactic shock | 25 | 6.1% | 0 | 8 |
| Maternal exposure during pregnancy | 25 | 6.1% | 0 | 16 |
| Haemorrhage foetal | 24 | 5.9% | 0 | 24 |
| Blood pressure increased | 22 | 5.4% | 0 | 1 |
| Haemorrhage | 21 | 5.2% | 3 | 3 |
| Hypertension | 19 | 4.7% | 1 | 2 |
| Anaphylactic reaction | 18 | 4.4% | 0 | 1 |
Other Indications for FIBRINOGEN HUMAN
Product used for unknown indication (67)
Factor i deficiency (35)
Haemorrhage (35)
Congenital dysfibrinogenaemia (30)
Drug therapy (25)
Postpartum haemorrhage (17)
Procedural haemorrhage (17)
Prophylaxis (16)
Foetal exposure during pregnancy (11)
Haemorrhage prophylaxis (11)