Does ELBASVIR\GRAZOPREVIR Cause Product dose omission? 23 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 23 reports of Product dose omission have been filed in association with ELBASVIR\GRAZOPREVIR. This represents 0.6% of all adverse event reports for ELBASVIR\GRAZOPREVIR.
23
Reports of Product dose omission with ELBASVIR\GRAZOPREVIR
0.6%
of all ELBASVIR\GRAZOPREVIR reports
1
Deaths
1
Hospitalizations
How Dangerous Is Product dose omission From ELBASVIR\GRAZOPREVIR?
Of the 23 reports, 1 (4.3%) resulted in death, 1 (4.3%) required hospitalization, and 1 (4.3%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ELBASVIR\GRAZOPREVIR. However, 23 reports have been filed with the FAERS database.
What Other Side Effects Does ELBASVIR\GRAZOPREVIR Cause?
Fatigue (912)
Headache (704)
Nausea (447)
Drug dose omission (254)
Diarrhoea (253)
Insomnia (195)
Hepatitis c (175)
Vomiting (145)
Adverse event (134)
Dizziness (119)
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 ELBASVIR\GRAZOPREVIR Alternatives Have Lower Product dose omission Risk?
ELBASVIR\GRAZOPREVIR vs ELDECALCITOL
ELBASVIR\GRAZOPREVIR vs ELECTROLYTES NOS
ELBASVIR\GRAZOPREVIR vs ELECTROLYTES NOS\MINERALS
ELBASVIR\GRAZOPREVIR vs ELETRIPTAN
ELBASVIR\GRAZOPREVIR vs ELETRIPTAN HYDROBROMIDE