Does DOLUTEGRAVIR\LAMIVUDINE Cause Condition aggravated? 53 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 53 reports of Condition aggravated have been filed in association with DOLUTEGRAVIR\LAMIVUDINE. This represents 1.7% of all adverse event reports for DOLUTEGRAVIR\LAMIVUDINE.
53
Reports of Condition aggravated with DOLUTEGRAVIR\LAMIVUDINE
1.7%
of all DOLUTEGRAVIR\LAMIVUDINE reports
1
Deaths
11
Hospitalizations
How Dangerous Is Condition aggravated From DOLUTEGRAVIR\LAMIVUDINE?
Of the 53 reports, 1 (1.9%) resulted in death, 11 (20.8%) required hospitalization.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DOLUTEGRAVIR\LAMIVUDINE. However, 53 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which DOLUTEGRAVIR\LAMIVUDINE Alternatives Have Lower Condition aggravated 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