Does SOFOSBUVIR\VELPATASVIR Cause Product dose omission issue? 625 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 625 reports of Product dose omission issue have been filed in association with SOFOSBUVIR\VELPATASVIR. This represents 3.5% of all adverse event reports for SOFOSBUVIR\VELPATASVIR.
625
Reports of Product dose omission issue with SOFOSBUVIR\VELPATASVIR
3.5%
of all SOFOSBUVIR\VELPATASVIR reports
1
Deaths
69
Hospitalizations
How Dangerous Is Product dose omission issue From SOFOSBUVIR\VELPATASVIR?
Of the 625 reports, 1 (0.2%) resulted in death, 69 (11.0%) required hospitalization.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOFOSBUVIR\VELPATASVIR. However, 625 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)
Death (597)
Hepatitis c (510)
Vomiting (507)
Intentional dose omission (474)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which SOFOSBUVIR\VELPATASVIR Alternatives Have Lower Product dose omission issue Risk?
SOFOSBUVIR\VELPATASVIR vs SOFOSBUVIR\VELPATASVIR\VOXILAPREVIR
SOFOSBUVIR\VELPATASVIR vs SOLIFENACIN
SOFOSBUVIR\VELPATASVIR vs SOLIRIS
SOFOSBUVIR\VELPATASVIR vs SOLOSTAR
SOFOSBUVIR\VELPATASVIR vs SOLRIAMFETOL