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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125558661 | 12555866 | 1 | I | 201601 | 20160701 | 20160714 | 20160714 | EXP | GB-MHRA-EYC 00141641 | GB-TEVA-674254ACC | TEVA | 35.00 | YR | F | Y | 0.00000 | 20160714 | PH | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125558661 | 12555866 | 1 | PS | NAPROXEN. | NAPROXEN | 1 | Oral | 1000 MILLIGRAM DAILY; | 22000 | MG | U | U | 74129 | 500 | MG | BID | |||
| 125558661 | 12555866 | 2 | C | PARACETAMOL AND DIHYDROCODEINE | 2 | 0 | |||||||||||||
| 125558661 | 12555866 | 3 | C | ESOMEPRAZOLE | ESOMEPRAZOLE | 1 | 0 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125558661 | 12555866 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125558661 | 12555866 | Abdominal distension | |
| 125558661 | 12555866 | Anaemia | |
| 125558661 | 12555866 | Dyspnoea | |
| 125558661 | 12555866 | Gastrooesophageal reflux disease | |
| 125558661 | 12555866 | Malaise | |
| 125558661 | 12555866 | Sensation of foreign body |
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 |
|---|---|---|---|---|---|---|
| 125558661 | 12555866 | 1 | 20151210 | 0 |