Does DOLUTEGRAVIR\LAMIVUDINE Cause Extra dose administered? 49 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 49 reports of Extra dose administered have been filed in association with DOLUTEGRAVIR\LAMIVUDINE. This represents 1.5% of all adverse event reports for DOLUTEGRAVIR\LAMIVUDINE.
49
Reports of Extra dose administered with DOLUTEGRAVIR\LAMIVUDINE
1.5%
of all DOLUTEGRAVIR\LAMIVUDINE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Extra dose administered From DOLUTEGRAVIR\LAMIVUDINE?
Of the 49 reports, 2 (4.1%) required hospitalization.
Is Extra dose administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DOLUTEGRAVIR\LAMIVUDINE. However, 49 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)
Intentional dose omission (112)
Viral load increased (104)
Rash (99)
Treatment noncompliance (97)
What Other Drugs Cause Extra dose administered?
TIRZEPATIDE (6,774)
DULAGLUTIDE (3,047)
LORATADINE (1,556)
DUPILUMAB (1,422)
FEXOFENADINE (1,413)
NAPROXEN (908)
POLYETHYLENE GLYCOL 3350 (589)
ACETAMINOPHEN (552)
DALFAMPRIDINE (519)
FLUTICASONE\SALMETEROL (499)
Which DOLUTEGRAVIR\LAMIVUDINE Alternatives Have Lower Extra dose administered 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