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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 Full blood count abnormal? 103 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 103 reports of Full blood count abnormal have been filed in association with OLAPARIB (Lynparza). This represents 0.6% of all adverse event reports for OLAPARIB.

103
Reports of Full blood count abnormal with OLAPARIB
0.6%
of all OLAPARIB reports
3
Deaths
21
Hospitalizations

How Dangerous Is Full blood count abnormal From OLAPARIB?

Of the 103 reports, 3 (2.9%) resulted in death, 21 (20.4%) required hospitalization, and 2 (1.9%) were considered life-threatening.

Is Full blood count abnormal Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for OLAPARIB. However, 103 reports have been filed with the FAERS database.

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 Full blood count abnormal?

ALBUTEROL (3,060) PREDNISONE (2,230) BUDESONIDE\FORMOTEROL (1,786) TIOTROPIUM (1,754) MONTELUKAST (1,529) MEPOLIZUMAB (1,440) BUDESONIDE (1,339) PALBOCICLIB (1,146) CICLESONIDE (916) PANTOPRAZOLE (776)

Which OLAPARIB Alternatives Have Lower Full blood count abnormal 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 Full blood count abnormal Reports All Drugs Causing Full blood count abnormal OLAPARIB Demographics