Does OLMESARTAN MEDOXOMIL Cause Product administration error? 314 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 314 reports of Product administration error have been filed in association with OLMESARTAN MEDOXOMIL (OLMESARTAN MEDOXOMIL). This represents 2.6% of all adverse event reports for OLMESARTAN MEDOXOMIL.
314
Reports of Product administration error with OLMESARTAN MEDOXOMIL
2.6%
of all OLMESARTAN MEDOXOMIL reports
8
Deaths
231
Hospitalizations
How Dangerous Is Product administration error From OLMESARTAN MEDOXOMIL?
Of the 314 reports, 8 (2.5%) resulted in death, 231 (73.6%) required hospitalization, and 1 (0.3%) were considered life-threatening.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for OLMESARTAN MEDOXOMIL. However, 314 reports have been filed with the FAERS database.
What Other Side Effects Does OLMESARTAN MEDOXOMIL Cause?
Sprue-like enteropathy (3,482)
Gastrooesophageal reflux disease (1,819)
Acute kidney injury (1,587)
Weight decreased (1,569)
Haemorrhoids (1,316)
Diarrhoea (1,300)
Hiatus hernia (938)
Dizziness (885)
Large intestine polyp (839)
Constipation (796)
What Other Drugs Cause Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
ASPIRIN (241)
SECUKINUMAB (225)
HYDROCHLOROTHIAZIDE\OLMESARTAN MEDOXOMIL (222)
Which OLMESARTAN MEDOXOMIL Alternatives Have Lower Product administration error Risk?
OLMESARTAN MEDOXOMIL vs OLMETEC
OLMESARTAN MEDOXOMIL vs OLODATEROL
OLMESARTAN MEDOXOMIL vs OLODATEROL\TIOTROPIUM
OLMESARTAN MEDOXOMIL vs OLOPATADINE
OLMESARTAN MEDOXOMIL vs OLUTASIDENIB