Does REMDESIVIR Cause Recalled product administered? 59 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 59 reports of Recalled product administered have been filed in association with REMDESIVIR (Veklury). This represents 0.6% of all adverse event reports for REMDESIVIR.
59
Reports of Recalled product administered with REMDESIVIR
0.6%
of all REMDESIVIR reports
12
Deaths
6
Hospitalizations
How Dangerous Is Recalled product administered From REMDESIVIR?
Of the 59 reports, 12 (20.3%) resulted in death, 6 (10.2%) required hospitalization, and 2 (3.4%) were considered life-threatening.
Is Recalled product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for REMDESIVIR. However, 59 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 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 REMDESIVIR Alternatives Have Lower Recalled product administered Risk?
REMDESIVIR vs REMERON
REMDESIVIR vs REMICADE
REMDESIVIR vs REMIFENTANIL
REMDESIVIR vs REMIMAZOLAM
REMDESIVIR vs REMODULIN