Does REMDESIVIR Cause Condition aggravated? 318 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 318 reports of Condition aggravated have been filed in association with REMDESIVIR (Veklury). This represents 3.0% of all adverse event reports for REMDESIVIR.
318
Reports of Condition aggravated with REMDESIVIR
3.0%
of all REMDESIVIR reports
133
Deaths
93
Hospitalizations
How Dangerous Is Condition aggravated From REMDESIVIR?
Of the 318 reports, 133 (41.8%) resulted in death, 93 (29.2%) required hospitalization, and 46 (14.5%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for REMDESIVIR. However, 318 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which REMDESIVIR Alternatives Have Lower Condition aggravated Risk?
REMDESIVIR vs REMERON
REMDESIVIR vs REMICADE
REMDESIVIR vs REMIFENTANIL
REMDESIVIR vs REMIMAZOLAM
REMDESIVIR vs REMODULIN