Does VERAPAMIL Cause Product administration error? 27 Reports in FDA Database
Lower Your Cholesterol — The Natural Way
The Oxidized Cholesterol Strategy: a science-backed plan for heart health.
According to the FDA Adverse Event Reporting System (FAERS), 27 reports of Product administration error have been filed in association with VERAPAMIL (Verapamil Hydrochloride). This represents 0.3% of all adverse event reports for VERAPAMIL.
27
Reports of Product administration error with VERAPAMIL
0.3%
of all VERAPAMIL reports
7
Deaths
8
Hospitalizations
How Dangerous Is Product administration error From VERAPAMIL?
Of the 27 reports, 7 (25.9%) resulted in death, 8 (29.6%) required hospitalization, and 5 (18.5%) 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 VERAPAMIL. However, 27 reports have been filed with the FAERS database.
What Other Side Effects Does VERAPAMIL Cause?
Completed suicide (1,274)
Toxicity to various agents (1,048)
Drug ineffective (917)
Hypotension (897)
Bradycardia (690)
Off label use (578)
Dyspnoea (563)
Dizziness (548)
Drug interaction (521)
Nausea (506)
What Other Drugs Cause Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which VERAPAMIL Alternatives Have Lower Product administration error Risk?
VERAPAMIL vs VERICIGUAT
VERAPAMIL vs VERTEPORFIN
VERAPAMIL vs VESICARE
VERAPAMIL vs VFEND
VERAPAMIL vs VIAGRA