Does DULAGLUTIDE Cause Haemoglobin decreased? 28 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 28 reports of Haemoglobin decreased have been filed in association with DULAGLUTIDE (Trulicity). This represents 0.0% of all adverse event reports for DULAGLUTIDE.
28
Reports of Haemoglobin decreased with DULAGLUTIDE
0.0%
of all DULAGLUTIDE reports
2
Deaths
16
Hospitalizations
How Dangerous Is Haemoglobin decreased From DULAGLUTIDE?
Of the 28 reports, 2 (7.1%) resulted in death, 16 (57.1%) required hospitalization, and 1 (3.6%) were considered life-threatening.
Is Haemoglobin decreased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULAGLUTIDE. However, 28 reports have been filed with the FAERS database.
What Other Side Effects Does DULAGLUTIDE Cause?
Injection site pain (9,474)
Nausea (9,137)
Blood glucose increased (9,119)
Incorrect dose administered (5,207)
Diarrhoea (5,036)
Vomiting (4,880)
Inappropriate schedule of product administration (3,606)
Extra dose administered (3,047)
Injection site haemorrhage (3,028)
Weight decreased (3,000)
What Other Drugs Cause Haemoglobin decreased?
LENALIDOMIDE (4,031)
RUXOLITINIB (3,297)
ECULIZUMAB (3,028)
ADALIMUMAB (2,459)
CLOZAPINE (2,396)
RITUXIMAB (1,803)
APIXABAN (1,779)
NIRAPARIB (1,759)
METHOTREXATE (1,754)
RIBAVIRIN (1,753)
Which DULAGLUTIDE Alternatives Have Lower Haemoglobin decreased Risk?
DULAGLUTIDE vs DULERA
DULAGLUTIDE vs DULOXETINE
DULAGLUTIDE vs DUPILUMAB
DULAGLUTIDE vs DURAGESIC
DULAGLUTIDE vs DUROGESIC