Does REMDESIVIR Cause Wrong technique in product usage process? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Wrong technique in product usage process have been filed in association with REMDESIVIR (Veklury). This represents 0.1% of all adverse event reports for REMDESIVIR.
9
Reports of Wrong technique in product usage process with REMDESIVIR
0.1%
of all REMDESIVIR reports
1
Deaths
2
Hospitalizations
How Dangerous Is Wrong technique in product usage process From REMDESIVIR?
Of the 9 reports, 1 (11.1%) resulted in death, 2 (22.2%) required hospitalization.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for REMDESIVIR. However, 9 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which REMDESIVIR Alternatives Have Lower Wrong technique in product usage process Risk?
REMDESIVIR vs REMERON
REMDESIVIR vs REMICADE
REMDESIVIR vs REMIFENTANIL
REMDESIVIR vs REMIMAZOLAM
REMDESIVIR vs REMODULIN