Does ACYCLOVIR Cause Incorrect product administration duration? 30 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 30 reports of Incorrect product administration duration have been filed in association with ACYCLOVIR (Acyclovir). This represents 0.2% of all adverse event reports for ACYCLOVIR.
30
Reports of Incorrect product administration duration with ACYCLOVIR
0.2%
of all ACYCLOVIR reports
5
Deaths
15
Hospitalizations
How Dangerous Is Incorrect product administration duration From ACYCLOVIR?
Of the 30 reports, 5 (16.7%) resulted in death, 15 (50.0%) required hospitalization, and 2 (6.7%) 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 ACYCLOVIR. However, 30 reports have been filed with the FAERS database.
What Other Side Effects Does ACYCLOVIR Cause?
Drug ineffective (1,727)
Acute kidney injury (1,405)
Off label use (942)
Headache (694)
Condition aggravated (584)
Pyrexia (565)
Nausea (537)
Rash (461)
Neurotoxicity (460)
Dyspnoea (446)
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 ACYCLOVIR Alternatives Have Lower Incorrect product administration duration Risk?
ACYCLOVIR vs AD26.COV2.S
ACYCLOVIR vs ADAGRASIB
ACYCLOVIR vs ADALIMUMAB
ACYCLOVIR vs ADALIMUMAB-AACF
ACYCLOVIR vs ADALIMUMAB-AATY