Does SOFOSBUVIR\VELPATASVIR Cause Product dose omission? 364 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 364 reports of Product dose omission have been filed in association with SOFOSBUVIR\VELPATASVIR. This represents 2.0% of all adverse event reports for SOFOSBUVIR\VELPATASVIR.
364
Reports of Product dose omission with SOFOSBUVIR\VELPATASVIR
2.0%
of all SOFOSBUVIR\VELPATASVIR reports
0
Deaths
31
Hospitalizations
How Dangerous Is Product dose omission From SOFOSBUVIR\VELPATASVIR?
Of the 364 reports, 31 (8.5%) 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 SOFOSBUVIR\VELPATASVIR. However, 364 reports have been filed with the FAERS database.
What Other Side Effects Does SOFOSBUVIR\VELPATASVIR Cause?
Fatigue (3,666)
Headache (3,084)
Nausea (1,637)
Diarrhoea (882)
Insomnia (715)
Drug ineffective (694)
Product dose omission issue (625)
Death (597)
Hepatitis c (510)
Vomiting (507)
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 SOFOSBUVIR\VELPATASVIR Alternatives Have Lower Product dose omission Risk?
SOFOSBUVIR\VELPATASVIR vs SOFOSBUVIR\VELPATASVIR\VOXILAPREVIR
SOFOSBUVIR\VELPATASVIR vs SOLIFENACIN
SOFOSBUVIR\VELPATASVIR vs SOLIRIS
SOFOSBUVIR\VELPATASVIR vs SOLOSTAR
SOFOSBUVIR\VELPATASVIR vs SOLRIAMFETOL