Does VERAPAMIL Cause Wrong technique in product usage process? 40 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 40 reports of Wrong technique in product usage process have been filed in association with VERAPAMIL (Verapamil Hydrochloride). This represents 0.4% of all adverse event reports for VERAPAMIL.
40
Reports of Wrong technique in product usage process with VERAPAMIL
0.4%
of all VERAPAMIL reports
0
Deaths
2
Hospitalizations
How Dangerous Is Wrong technique in product usage process From VERAPAMIL?
Of the 40 reports, 2 (5.0%) required hospitalization, and 1 (2.5%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VERAPAMIL. However, 40 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which VERAPAMIL Alternatives Have Lower Wrong technique in product usage process Risk?
VERAPAMIL vs VERICIGUAT
VERAPAMIL vs VERTEPORFIN
VERAPAMIL vs VESICARE
VERAPAMIL vs VFEND
VERAPAMIL vs VIAGRA