Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 119804707 | 11980470 | 7 | F | 20160804 | 20160129 | 20160811 | EXP | US-PFIZER INC-2016031700 | PFIZER | 72.00 | YR | M | Y | 85.00000 | KG | 20160811 | MD | US | US |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 119804707 | 11980470 | 1 | PS | SUTENT | SUNITINIB MALATE | 1 | 12.5 MG, CYCLIC (28 DAYS ON/14 DAYS OFF) | N | 21938 | 12.5 | MG | CAPSULE, HARD | |||||||
| 119804707 | 11980470 | 2 | C | METOPROLOL. | METOPROLOL | 1 | UNK | 0 | |||||||||||
| 119804707 | 11980470 | 3 | C | LIPITOR | ATORVASTATIN CALCIUM | 1 | UNK | 0 | |||||||||||
| 119804707 | 11980470 | 4 | C | FLOMAX | TAMSULOSIN HYDROCHLORIDE | 1 | UNK | 0 | |||||||||||
| 119804707 | 11980470 | 5 | C | TYLENOL | ACETAMINOPHEN | 1 | UNK | 0 | |||||||||||
| 119804707 | 11980470 | 6 | C | CALCIUM | CALCIUM | 1 | UNK | 0 | |||||||||||
| 119804707 | 11980470 | 7 | C | PRILOSEC | OMEPRAZOLE MAGNESIUM | 1 | UNK | 0 | |||||||||||
| 119804707 | 11980470 | 8 | C | INSULIN | INSULIN NOS | 1 | UNK (INSULIN 75/25) | 0 | |||||||||||
| 119804707 | 11980470 | 9 | C | COMBIVENT | ALBUTEROL SULFATEIPRATROPIUM BROMIDE | 1 | UNK | 0 | |||||||||||
| 119804707 | 11980470 | 10 | C | BENADRYL | DIPHENHYDRAMINE HYDROCHLORIDE | 1 | UNK | 0 | |||||||||||
| 119804707 | 11980470 | 11 | C | TYLENOL PM | ACETAMINOPHENDIPHENHYDRAMINE | 1 | UNK | 0 | |||||||||||
| 119804707 | 11980470 | 12 | C | PLETAL | CILOSTAZOL | 1 | UNK | 0 | |||||||||||
| 119804707 | 11980470 | 13 | C | AVODART | DUTASTERIDE | 1 | UNK | 0 | |||||||||||
| 119804707 | 11980470 | 14 | C | GLUCOSE | DEXTROSE | 1 | UNK | 0 | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 119804707 | 11980470 | 1 | Metastatic renal cell carcinoma |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 119804707 | 11980470 | OT |
| 119804707 | 11980470 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 119804707 | 11980470 | Anaemia | |
| 119804707 | 11980470 | Asthenia | |
| 119804707 | 11980470 | Blood calcium abnormal | |
| 119804707 | 11980470 | Bradyphrenia | |
| 119804707 | 11980470 | Chest pain | |
| 119804707 | 11980470 | Constipation | |
| 119804707 | 11980470 | Diarrhoea | |
| 119804707 | 11980470 | Dyspnoea | |
| 119804707 | 11980470 | Fall | |
| 119804707 | 11980470 | Fatigue | |
| 119804707 | 11980470 | Full blood count decreased | |
| 119804707 | 11980470 | Haemorrhage | |
| 119804707 | 11980470 | Head injury | |
| 119804707 | 11980470 | Heart rate abnormal | |
| 119804707 | 11980470 | Hypervolaemia | |
| 119804707 | 11980470 | Hypotension | |
| 119804707 | 11980470 | Insomnia | |
| 119804707 | 11980470 | Nausea | |
| 119804707 | 11980470 | Pneumonia | |
| 119804707 | 11980470 | Pulmonary oedema | |
| 119804707 | 11980470 | Restlessness | |
| 119804707 | 11980470 | Scratch | |
| 119804707 | 11980470 | Skin abrasion | |
| 119804707 | 11980470 | Thrombosis |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 119804707 | 11980470 | 1 | 20160115 | 20160802 | 0 |