Does REMDESIVIR Cause Recalled product? 36 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 36 reports of Recalled product have been filed in association with REMDESIVIR (Veklury). This represents 0.3% of all adverse event reports for REMDESIVIR.
36
Reports of Recalled product with REMDESIVIR
0.3%
of all REMDESIVIR reports
8
Deaths
3
Hospitalizations
How Dangerous Is Recalled product From REMDESIVIR?
Of the 36 reports, 8 (22.2%) resulted in death, 3 (8.3%) required hospitalization.
Is Recalled product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for REMDESIVIR. However, 36 reports have been filed with the FAERS database.
What Other Side Effects Does REMDESIVIR Cause?
Off label use (1,092)
Alanine aminotransferase increased (1,047)
Death (808)
Aspartate aminotransferase increased (713)
Bradycardia (652)
Acute kidney injury (605)
Covid-19 (570)
Drug ineffective (497)
Liver function test increased (447)
Respiratory failure (394)
What Other Drugs Cause Recalled product?
PARATHYROID HORMONE (900)
ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT (80)
CALCITRIOL (68)
CALCIUM (66)
LEVOTHYROXINE\LIOTHYRONINE (34)
TESTOSTERONE (32)
VALSARTAN (32)
CHLORHEXIDINE (28)
ALCOHOL (26)
LEVOTHYROXINE (24)
Which REMDESIVIR Alternatives Have Lower Recalled product Risk?
REMDESIVIR vs REMERON
REMDESIVIR vs REMICADE
REMDESIVIR vs REMIFENTANIL
REMDESIVIR vs REMIMAZOLAM
REMDESIVIR vs REMODULIN