Does DOLUTEGRAVIR\LAMIVUDINE Cause Intentional dose omission? 112 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 112 reports of Intentional dose omission have been filed in association with DOLUTEGRAVIR\LAMIVUDINE. This represents 3.5% of all adverse event reports for DOLUTEGRAVIR\LAMIVUDINE.
112
Reports of Intentional dose omission with DOLUTEGRAVIR\LAMIVUDINE
3.5%
of all DOLUTEGRAVIR\LAMIVUDINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Intentional dose omission From DOLUTEGRAVIR\LAMIVUDINE?
Of the 112 reports.
Is Intentional dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DOLUTEGRAVIR\LAMIVUDINE. However, 112 reports have been filed with the FAERS database.
What Other Side Effects Does DOLUTEGRAVIR\LAMIVUDINE Cause?
Product dose omission issue (1,089)
Inappropriate schedule of product administration (256)
Product dose omission in error (234)
Product use issue (194)
Drug ineffective (137)
Pathogen resistance (137)
Viral load increased (104)
Rash (99)
Treatment noncompliance (97)
Viral mutation identified (94)
What Other Drugs Cause Intentional dose omission?
DUPILUMAB (2,269)
CERTOLIZUMAB PEGOL (1,253)
ADALIMUMAB (845)
TOFACITINIB (845)
INFLIXIMAB (815)
ABALOPARATIDE (623)
ETANERCEPT (615)
AMBRISENTAN (595)
SODIUM OXYBATE (580)
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)
Which DOLUTEGRAVIR\LAMIVUDINE Alternatives Have Lower Intentional dose omission Risk?
DOLUTEGRAVIR\LAMIVUDINE vs DOLUTEGRAVIR\LAMIVUDINE\TENOFOVIR DISOPROXIL
DOLUTEGRAVIR\LAMIVUDINE vs DOLUTEGRAVIR\RILPIVIRINE
DOLUTEGRAVIR\LAMIVUDINE vs DOMPERIDONE
DOLUTEGRAVIR\LAMIVUDINE vs DOMPERIDONE\PANTOPRAZOLE
DOLUTEGRAVIR\LAMIVUDINE vs DONANEMAB-AZBT