Does CANDESARTAN Cause Product quality issue? 493 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 493 reports of Product quality issue have been filed in association with CANDESARTAN. This represents 5.5% of all adverse event reports for CANDESARTAN.
493
Reports of Product quality issue with CANDESARTAN
5.5%
of all CANDESARTAN reports
492
Deaths
405
Hospitalizations
How Dangerous Is Product quality issue From CANDESARTAN?
Of the 493 reports, 492 (99.8%) resulted in death, 405 (82.2%) required hospitalization, and 420 (85.2%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CANDESARTAN. However, 493 reports have been filed with the FAERS database.
What Other Side Effects Does CANDESARTAN Cause?
Off label use (1,911)
Fatigue (1,468)
Dyspnoea (1,456)
Pain (1,455)
Drug ineffective (1,428)
Headache (1,371)
Nausea (1,282)
Dizziness (1,237)
Vomiting (1,202)
Diarrhoea (1,145)
What Other Drugs Cause Product quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which CANDESARTAN Alternatives Have Lower Product quality issue Risk?
CANDESARTAN vs CANDESARTAN CILEXETIL
CANDESARTAN vs CANDESARTAN CILEXETIL\HYDROCHLOROTHIAZIDE
CANDESARTAN vs CANGRELOR
CANDESARTAN vs CANIS LUPUS FAMILIARIS SKIN
CANDESARTAN vs CANNABIDIOL