Does REMDESIVIR Cause Product preparation issue? 40 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 40 reports of Product preparation issue have been filed in association with REMDESIVIR (Veklury). This represents 0.4% of all adverse event reports for REMDESIVIR.
40
Reports of Product preparation issue with REMDESIVIR
0.4%
of all REMDESIVIR reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product preparation issue From REMDESIVIR?
Of the 40 reports, 3 (7.5%) required hospitalization.
Is Product preparation issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for REMDESIVIR. However, 40 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 preparation issue?
ONABOTULINUMTOXINA (677)
COAGULATION FACTOR IX HUMAN\COAGULATION FACTOR VII HUMAN\COAGULATION FACTOR X HUMAN\PROTEIN C\PROTEIN S HUMAN\PROTHROMBIN (252)
HUMAN C1-ESTERASE INHIBITOR (238)
SOMATROPIN (200)
INCOBOTULINUMTOXINA (174)
STIRIPENTOL (129)
TESAMORELIN (119)
ABATACEPT (115)
INFLIXIMAB (101)
ABOBOTULINUMTOXINA (91)
Which REMDESIVIR Alternatives Have Lower Product preparation issue Risk?
REMDESIVIR vs REMERON
REMDESIVIR vs REMICADE
REMDESIVIR vs REMIFENTANIL
REMDESIVIR vs REMIMAZOLAM
REMDESIVIR vs REMODULIN