Rucaparib
Common brands: Rubraca, Vitamin D, Neurontin, Ondansetron, Gralise
Top reporter: Pharmaand Gmbh
Benzodiazepine [EPC]Nonsteroidal Anti-inflammatory Drug [EPC]Provitamin D2 Compound [EPC]Serotonin-3 Receptor Antagonist [EPC]Programmed Death Receptor-1 Blocking Antibody [EPC]
8,760
Total Reports
2,777
Serious Reports
502
Death Reports
30
Reported Reactions
Death Report Ratio: High (5.73%)
Patient Demographics
Reported Adverse Reactions (30)
Side effects reported in FDA adverse event reports for Rucaparib.
| # | Reaction | Reports | % of Total |
|---|---|---|---|
| 1 | FATIGUE | 2,547 | |
| 2 | NAUSEA | 2,258 | |
| 3 | MALIGNANT NEOPLASM PROGRESSION | 1,184 | |
| 4 | DECREASED APPETITE | 802 | |
| 5 | DIARRHOEA | 789 | |
| 6 | CONSTIPATION | 783 | |
| 7 | VOMITING | 780 | |
| 8 | ASTHENIA | 679 | |
| 9 | ADVERSE EVENT | 571 | |
| 10 | CARBOHYDRATE ANTIGEN 125 INCREASED | 569 | |
| 11 | DYSGEUSIA | 565 | |
| 12 | ANAEMIA | 553 | |
| 13 | PRODUCT DOSE OMISSION ISSUE | 550 | |
| 14 | PLATELET COUNT DECREASED | 539 | |
| 15 | DRUG INEFFECTIVE | 519 | |
| 16 | HEADACHE | 437 | |
| 17 | MALAISE | 410 | |
| 18 | DIZZINESS | 407 | |
| 19 | DYSPNOEA | 397 | |
| 20 | ABDOMINAL PAIN | 388 | |
| 21 | ABDOMINAL PAIN UPPER | 367 | |
| 22 | PRODUCT DOSE OMISSION | 362 | |
| 23 | HAEMOGLOBIN DECREASED | 359 | |
| 24 | DEATH | 351 | |
| 25 | ABDOMINAL DISCOMFORT | 349 | |
| 26 | WHITE BLOOD CELL COUNT DECREASED | 315 | |
| 27 | WEIGHT DECREASED | 296 | |
| 28 | PAIN | 295 | |
| 29 | RED BLOOD CELL COUNT DECREASED | 288 | |
| 30 | OFF LABEL USE | 274 |
Important Disclaimer
FDA adverse event reports are submitted voluntarily and do not prove causation. A reported reaction does not mean the drug caused it. Drugs with more users naturally have more reports. Always consult your doctor or pharmacist before making medication decisions.