Does VALACYCLOVIR Cause Incorrect product administration duration? 35 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 35 reports of Incorrect product administration duration have been filed in association with VALACYCLOVIR (Valacyclovir Hydrochloride). This represents 0.3% of all adverse event reports for VALACYCLOVIR.
35
Reports of Incorrect product administration duration with VALACYCLOVIR
0.3%
of all VALACYCLOVIR reports
5
Deaths
21
Hospitalizations
How Dangerous Is Incorrect product administration duration From VALACYCLOVIR?
Of the 35 reports, 5 (14.3%) resulted in death, 21 (60.0%) required hospitalization, and 3 (8.6%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VALACYCLOVIR. However, 35 reports have been filed with the FAERS database.
What Other Side Effects Does VALACYCLOVIR Cause?
Acute kidney injury (978)
Drug ineffective (894)
Off label use (593)
Pyrexia (551)
Drug reaction with eosinophilia and systemic symptoms (496)
Confusional state (456)
Rash (423)
Nausea (415)
Neurotoxicity (404)
Altered state of consciousness (395)
What Other Drugs Cause Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which VALACYCLOVIR Alternatives Have Lower Incorrect product administration duration Risk?
VALACYCLOVIR vs VALBENAZINE
VALACYCLOVIR vs VALBENAZINE DITOSYLATE
VALACYCLOVIR vs VALDECOXIB
VALACYCLOVIR vs VALERIAN
VALACYCLOVIR vs VALGANCICLOVIR