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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126767601 | 12676760 | 1 | I | 201606 | 20160812 | 20160823 | 20160823 | EXP | GB-MHRA-ADR 23595376 | GB-SA-2016SA149771 | AVENTIS | 81.00 | YR | E | F | Y | 63.50000 | KG | 20160823 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126767601 | 12676760 | 1 | PS | INDAPAMIDE. | INDAPAMIDE | 1 | Unknown | TAKEN FOR 3/4 DAYS ONLY. | Y | U | 18538 | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126767601 | 12676760 | 1 | Hypertension |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126767601 | 12676760 | OT |
| 126767601 | 12676760 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126767601 | 12676760 | Balance disorder | |
| 126767601 | 12676760 | Confusional state | |
| 126767601 | 12676760 | Feeling abnormal | |
| 126767601 | 12676760 | Headache | |
| 126767601 | 12676760 | Hyponatraemia | |
| 126767601 | 12676760 | Syncope | |
| 126767601 | 12676760 | 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 |
|---|---|---|---|---|---|---|
| 126767601 | 12676760 | 1 | 201605 | 201605 | 0 |