Does CARVEDILOL Cause Wrong technique in product usage process? 227 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 227 reports of Wrong technique in product usage process have been filed in association with CARVEDILOL (Carvedilol Phosphate). This represents 1.7% of all adverse event reports for CARVEDILOL.
227
Reports of Wrong technique in product usage process with CARVEDILOL
1.7%
of all CARVEDILOL reports
6
Deaths
67
Hospitalizations
How Dangerous Is Wrong technique in product usage process From CARVEDILOL?
Of the 227 reports, 6 (2.6%) resulted in death, 67 (29.5%) required hospitalization, and 5 (2.2%) 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 CARVEDILOL. However, 227 reports have been filed with the FAERS database.
What Other Side Effects Does CARVEDILOL Cause?
Hypotension (1,822)
Dyspnoea (1,143)
Dizziness (1,138)
Drug ineffective (1,102)
Fatigue (1,020)
Completed suicide (1,019)
Bradycardia (861)
Toxicity to various agents (690)
Cardiac failure (636)
Asthenia (562)
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 CARVEDILOL Alternatives Have Lower Wrong technique in product usage process Risk?
CARVEDILOL vs CASIMERSEN
CARVEDILOL vs CASIRIVIMAB
CARVEDILOL vs CASIRIVIMAB\IMDEVIMAB
CARVEDILOL vs CASPOFUNGIN
CARVEDILOL vs CATEQUENTINIB