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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does OLAPARIB Cause Haemoglobin decreased? 390 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 390 reports of Haemoglobin decreased have been filed in association with OLAPARIB (Lynparza). This represents 2.1% of all adverse event reports for OLAPARIB.

390
Reports of Haemoglobin decreased with OLAPARIB
2.1%
of all OLAPARIB reports
34
Deaths
117
Hospitalizations

How Dangerous Is Haemoglobin decreased From OLAPARIB?

Of the 390 reports, 34 (8.7%) resulted in death, 117 (30.0%) required hospitalization, and 40 (10.3%) were considered life-threatening.

Is Haemoglobin decreased Listed in the Official Label?

Yes, Haemoglobin decreased is listed as a known adverse reaction in the official FDA drug label for OLAPARIB.

What Other Side Effects Does OLAPARIB Cause?

Death (4,378) Malignant neoplasm progression (1,862) Nausea (1,582) Anaemia (1,455) Fatigue (1,437) Off label use (777) Vomiting (642) Drug ineffective (563) Diarrhoea (514) Asthenia (491)

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 OLAPARIB Alternatives Have Lower Haemoglobin decreased Risk?

OLAPARIB vs OLARATUMAB OLAPARIB vs OLECLUMAB OLAPARIB vs OLIVE OIL\SOYBEAN OIL OLAPARIB vs OLMESARTAN OLAPARIB vs OLMESARTAN MEDOXOMIL

Related Pages

OLAPARIB Full Profile All Haemoglobin decreased Reports All Drugs Causing Haemoglobin decreased OLAPARIB Demographics