FIBRINOGEN HUMAN for Factor i deficiency: Side Effects & Safety Data

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There are 35 adverse event reports in the FDA FAERS database where FIBRINOGEN HUMAN was used for Factor i deficiency.

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