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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126678801 | 12667880 | 1 | I | 20160509 | 20160811 | 20160819 | 20160819 | EXP | GB-PURDUE-GBR-2016-0039995 | PURDUE | 63.00 | YR | F | Y | 100.00000 | KG | 20160818 | MD | GB | GB |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126678801 | 12667880 | 1 | PS | MST CONTINUS Tablets | MORPHINE SULFATE | 1 | Unknown | 20 MG, BID | Y | U | 19516 | 20 | MG | PROLONGED-RELEASE TABLET | |||||
| 126678801 | 12667880 | 2 | SS | NAPROXEN SODIUM. | NAPROXEN SODIUM | 1 | Oral | 250 MG, TID | Y | U | 0 | 250 | MG | ||||||
| 126678801 | 12667880 | 3 | SS | RAMIPRIL. | RAMIPRIL | 1 | Oral | 10 MG, DAILY | 0 | 10 | MG | ||||||||
| 126678801 | 12667880 | 4 | C | LANSOPRAZOLE. | LANSOPRAZOLE | 1 | U | 0 | |||||||||||
| 126678801 | 12667880 | 5 | C | LAXIDO | POLYETHYLENE GLYCOL 3350POTASSIUM CHLORIDESODIUM BICARBONATESODIUM CHLORIDE | 1 | U | 0 | |||||||||||
| 126678801 | 12667880 | 6 | C | LYRICA | PREGABALIN | 1 | U | 0 | |||||||||||
| 126678801 | 12667880 | 7 | C | PARACETAMOL | ACETAMINOPHEN | 1 | U | 0 | |||||||||||
| 126678801 | 12667880 | 8 | C | SERTRALINE | SERTRALINE HYDROCHLORIDE | 1 | U | 0 | |||||||||||
| 126678801 | 12667880 | 9 | C | SIMVASTATIN. | SIMVASTATIN | 1 | U | 0 | |||||||||||
| 126678801 | 12667880 | 10 | C | FLUTICASONE PROPIONATE W/SALMETEROL XINAFOATE | FLUTICASONE PROPIONATESALMETEROL XINAFOATE | 1 | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126678801 | 12667880 | 1 | Arthralgia |
| 126678801 | 12667880 | 2 | Arthralgia |
| 126678801 | 12667880 | 3 | Essential hypertension |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126678801 | 12667880 | HO |
| 126678801 | 12667880 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126678801 | 12667880 | Acute kidney injury | |
| 126678801 | 12667880 | Confusional state | |
| 126678801 | 12667880 | Coordination abnormal | |
| 126678801 | 12667880 | Diarrhoea | |
| 126678801 | 12667880 | Somnolence | |
| 126678801 | 12667880 | Toxicity to various agents | |
| 126678801 | 12667880 | 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 |
|---|---|---|---|---|---|---|
| 126678801 | 12667880 | 1 | 20141127 | 20160523 | 0 | |
| 126678801 | 12667880 | 2 | 20120223 | 20160523 | 0 | |
| 126678801 | 12667880 | 3 | 20090907 | 0 |