Does PEGINTERFERON LAMBDA-1A Cause Haemoglobin decreased? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Haemoglobin decreased have been filed in association with PEGINTERFERON LAMBDA-1A. This represents 8.6% of all adverse event reports for PEGINTERFERON LAMBDA-1A.
6
Reports of Haemoglobin decreased with PEGINTERFERON LAMBDA-1A
8.6%
of all PEGINTERFERON LAMBDA-1A reports
1
Deaths
2
Hospitalizations
How Dangerous Is Haemoglobin decreased From PEGINTERFERON LAMBDA-1A?
Of the 6 reports, 1 (16.7%) resulted in death, 2 (33.3%) required hospitalization, and 2 (33.3%) 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 PEGINTERFERON LAMBDA-1A. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does PEGINTERFERON LAMBDA-1A Cause?
Jaundice (18)
Rash (18)
Alanine aminotransferase increased (8)
Aspartate aminotransferase increased (8)
Hyperbilirubinaemia (7)
Pyrexia (7)
Ascites (6)
Hepatic failure (6)
Sleep disorder (6)
Affective disorder (5)
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)