Does CLOPIDOGREL BISULFATE Cause Incorrect product administration duration? 17 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 17 reports of Incorrect product administration duration have been filed in association with CLOPIDOGREL BISULFATE (Clopidogrel). This represents 0.0% of all adverse event reports for CLOPIDOGREL BISULFATE.
17
Reports of Incorrect product administration duration with CLOPIDOGREL BISULFATE
0.0%
of all CLOPIDOGREL BISULFATE reports
0
Deaths
11
Hospitalizations
How Dangerous Is Incorrect product administration duration From CLOPIDOGREL BISULFATE?
Of the 17 reports, 11 (64.7%) required hospitalization, and 5 (29.4%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CLOPIDOGREL BISULFATE. However, 17 reports have been filed with the FAERS database.
What Other Side Effects Does CLOPIDOGREL BISULFATE Cause?
Gastrointestinal haemorrhage (5,513)
Anaemia (3,043)
Dyspnoea (1,963)
Drug interaction (1,846)
Haemorrhage (1,762)
Drug ineffective (1,644)
Cerebral haemorrhage (1,603)
Dizziness (1,586)
Epistaxis (1,560)
Melaena (1,547)
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 CLOPIDOGREL BISULFATE Alternatives Have Lower Incorrect product administration duration Risk?
CLOPIDOGREL BISULFATE vs CLORAZEPATE
CLOPIDOGREL BISULFATE vs CLOSTRIDIUM TETANI TOXOID ANTIGEN
CLOPIDOGREL BISULFATE vs CLOTHIAPINE
CLOPIDOGREL BISULFATE vs CLOTIAZEPAM
CLOPIDOGREL BISULFATE vs CLOTRIMAZOLE