Does APREMILAST Cause Haemoglobin decreased? 54 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 54 reports of Haemoglobin decreased have been filed in association with APREMILAST (Otezla). This represents 0.0% of all adverse event reports for APREMILAST.
54
Reports of Haemoglobin decreased with APREMILAST
0.0%
of all APREMILAST reports
4
Deaths
21
Hospitalizations
How Dangerous Is Haemoglobin decreased From APREMILAST?
Of the 54 reports, 4 (7.4%) resulted in death, 21 (38.9%) required hospitalization, and 10 (18.5%) 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 APREMILAST. However, 54 reports have been filed with the FAERS database.
What Other Side Effects Does APREMILAST Cause?
Diarrhoea (23,752)
Nausea (21,352)
Psoriasis (19,255)
Headache (17,024)
Drug ineffective (14,121)
Abdominal discomfort (7,653)
Psoriatic arthropathy (7,035)
Vomiting (5,959)
Rash (5,883)
Pain (5,676)
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 APREMILAST Alternatives Have Lower Haemoglobin decreased Risk?
APREMILAST vs APREPITANT
APREMILAST vs APROTININ
APREMILAST vs ARANESP
APREMILAST vs ARAVA
APREMILAST vs AREDIA