Does REMDESIVIR Cause Product use issue? 98 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 98 reports of Product use issue have been filed in association with REMDESIVIR (Veklury). This represents 0.9% of all adverse event reports for REMDESIVIR.
98
Reports of Product use issue with REMDESIVIR
0.9%
of all REMDESIVIR reports
6
Deaths
13
Hospitalizations
How Dangerous Is Product use issue From REMDESIVIR?
Of the 98 reports, 6 (6.1%) resulted in death, 13 (13.3%) required hospitalization, and 1 (1.0%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for REMDESIVIR. However, 98 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 Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which REMDESIVIR Alternatives Have Lower Product use issue Risk?
REMDESIVIR vs REMERON
REMDESIVIR vs REMICADE
REMDESIVIR vs REMIFENTANIL
REMDESIVIR vs REMIMAZOLAM
REMDESIVIR vs REMODULIN