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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does ACYCLOVIR Cause Product dose omission? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Product dose omission have been filed in association with ACYCLOVIR (Acyclovir). This represents 0.0% of all adverse event reports for ACYCLOVIR.

6
Reports of Product dose omission with ACYCLOVIR
0.0%
of all ACYCLOVIR reports
0
Deaths
1
Hospitalizations

How Dangerous Is Product dose omission From ACYCLOVIR?

Of the 6 reports, 1 (16.7%) required hospitalization.

Is Product dose omission Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ACYCLOVIR. However, 6 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 Product dose omission?

APREMILAST (4,567) DUPILUMAB (2,729) ALBUTEROL (1,742) USTEKINUMAB (1,653) INSULIN GLARGINE (1,500) ETANERCEPT (1,400) LENALIDOMIDE (1,400) RUXOLITINIB (1,376) ALIROCUMAB (1,354) DIMETHYL (1,248)

Which ACYCLOVIR Alternatives Have Lower Product dose omission Risk?

ACYCLOVIR vs AD26.COV2.S ACYCLOVIR vs ADAGRASIB ACYCLOVIR vs ADALIMUMAB ACYCLOVIR vs ADALIMUMAB-AACF ACYCLOVIR vs ADALIMUMAB-AATY

Related Pages

ACYCLOVIR Full Profile All Product dose omission Reports All Drugs Causing Product dose omission ACYCLOVIR Demographics