Does PRASUGREL Cause Incorrect product administration duration? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Incorrect product administration duration have been filed in association with PRASUGREL (Prasugrel). This represents 0.1% of all adverse event reports for PRASUGREL.
5
Reports of Incorrect product administration duration with PRASUGREL
0.1%
of all PRASUGREL reports
0
Deaths
5
Hospitalizations
How Dangerous Is Incorrect product administration duration From PRASUGREL?
Of the 5 reports, 5 (100.0%) required hospitalization.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PRASUGREL. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does PRASUGREL Cause?
Gastrointestinal haemorrhage (401)
Haemorrhage (357)
Contusion (344)
Epistaxis (228)
Myocardial infarction (209)
Off label use (205)
Chest pain (204)
Dyspnoea (197)
Vascular stent thrombosis (159)
Dizziness (155)
What Other Drugs Cause Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which PRASUGREL Alternatives Have Lower Incorrect product administration duration Risk?
PRASUGREL vs PRAVASTATIN
PRASUGREL vs PRAVASTATIN\PRAVASTATIN
PRASUGREL vs PRAZAXA
PRASUGREL vs PRAZEPAM
PRASUGREL vs PRAZIQUANTEL