Does CARVEDILOL Cause Recalled product administered? 30 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 30 reports of Recalled product administered have been filed in association with CARVEDILOL (Carvedilol Phosphate). This represents 0.2% of all adverse event reports for CARVEDILOL.
30
Reports of Recalled product administered with CARVEDILOL
0.2%
of all CARVEDILOL reports
0
Deaths
5
Hospitalizations
How Dangerous Is Recalled product administered From CARVEDILOL?
Of the 30 reports, 5 (16.7%) required hospitalization.
Is Recalled product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CARVEDILOL. However, 30 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 Recalled product administered?
RAMIPRIL (1,028)
LISINOPRIL (744)
PENICILLIN G BENZATHINE (500)
LEVOTHYROXINE (406)
HUMAN IMMUNOGLOBULIN G (382)
VARENICLINE (381)
VALSARTAN (267)
QUINAPRIL (243)
TRIAMCINOLONE ACETONIDE (222)
RANITIDINE (204)
Which CARVEDILOL Alternatives Have Lower Recalled product administered Risk?
CARVEDILOL vs CASIMERSEN
CARVEDILOL vs CASIRIVIMAB
CARVEDILOL vs CASIRIVIMAB\IMDEVIMAB
CARVEDILOL vs CASPOFUNGIN
CARVEDILOL vs CATEQUENTINIB