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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122629066 | 12262906 | 6 | F | 2016 | 20160623 | 20160413 | 20160705 | EXP | US-PFIZER INC-2016195064 | PFIZER | 49.00 | YR | F | Y | 104.31000 | KG | 20160705 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122629066 | 12262906 | 1 | PS | SUTENT | SUNITINIB MALATE | 1 | 50 MG, CYCLIC (28 DAYS ON/14 DAYS OFF) | U | 21938 | 50 | MG | CAPSULE, HARD | |||||||
| 122629066 | 12262906 | 2 | C | AMLODIPINE | AMLODIPINE BESYLATE | 1 | UNK | 0 | |||||||||||
| 122629066 | 12262906 | 3 | C | HYDROCHLOROTHIAZIDE. | HYDROCHLOROTHIAZIDE | 1 | UNK | 0 | |||||||||||
| 122629066 | 12262906 | 4 | C | COZAAR | LOSARTAN POTASSIUM | 1 | UNK | 0 | |||||||||||
| 122629066 | 12262906 | 5 | C | PROTONIX | PANTOPRAZOLE SODIUM | 1 | UNK | 0 | |||||||||||
| 122629066 | 12262906 | 6 | C | ZOFRAN | ONDANSETRON HYDROCHLORIDE | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 122629066 | 12262906 | 1 | Gastrointestinal stromal tumour |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 122629066 | 12262906 | HO |
| 122629066 | 12262906 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 122629066 | 12262906 | Abdominal pain | |
| 122629066 | 12262906 | Asthenia | |
| 122629066 | 12262906 | Blister | |
| 122629066 | 12262906 | Blood pressure increased | |
| 122629066 | 12262906 | Chromaturia | |
| 122629066 | 12262906 | Dizziness | |
| 122629066 | 12262906 | Dyspepsia | |
| 122629066 | 12262906 | Eyelid oedema | |
| 122629066 | 12262906 | Fatigue | |
| 122629066 | 12262906 | Malaise | |
| 122629066 | 12262906 | Oral mucosal blistering | |
| 122629066 | 12262906 | Oral mucosal eruption | |
| 122629066 | 12262906 | Oral pain | |
| 122629066 | 12262906 | Pain | |
| 122629066 | 12262906 | Pain in extremity | |
| 122629066 | 12262906 | Stomatitis | |
| 122629066 | 12262906 | Swelling face | |
| 122629066 | 12262906 | Vomiting |
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 |
|---|---|---|---|---|---|---|
| 122629066 | 12262906 | 1 | 20160319 | 0 |