Does TIROFIBAN Cause Post procedural haemorrhage? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Post procedural haemorrhage have been filed in association with TIROFIBAN (AGGRASTAT). This represents 0.3% of all adverse event reports for TIROFIBAN.
6
Reports of Post procedural haemorrhage with TIROFIBAN
0.3%
of all TIROFIBAN reports
1
Deaths
0
Hospitalizations
How Dangerous Is Post procedural haemorrhage From TIROFIBAN?
Of the 6 reports, 1 (16.7%) resulted in death.
Is Post procedural haemorrhage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TIROFIBAN. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does TIROFIBAN Cause?
Haemorrhage (341)
Angina pectoris (177)
Haemorrhage intracranial (170)
Myocardial infarction (159)
Thrombocytopenia (150)
Cardiac failure acute (116)
Death (110)
Acute respiratory failure (99)
Cerebral haemorrhage (84)
Cardiac failure (68)
What Other Drugs Cause Post procedural haemorrhage?
LEVONORGESTREL (1,106)
RIVAROXABAN (930)
ASPIRIN (618)
APIXABAN (539)
ADALIMUMAB (476)
IBRUTINIB (269)
CLOPIDOGREL BISULFATE (235)
HEPARIN (174)
WARFARIN (170)
DABIGATRAN ETEXILATE (121)
Which TIROFIBAN Alternatives Have Lower Post procedural haemorrhage Risk?
TIROFIBAN vs TIRZEPATIDE
TIROFIBAN vs TISAGENLECLEUCEL
TIROFIBAN vs TISLELIZUMAB
TIROFIBAN vs TISOTUMAB VEDOTIN
TIROFIBAN vs TISOTUMAB VEDOTIN-TFTV