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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126740081 | 12674008 | 1 | I | 201606 | 20160812 | 20160822 | 20160822 | EXP | GB-MHRA-ADR 23595376 | GB-MYLANLABS-2016M1034075 | MYLAN | 0.00 | Y | 0.00000 | 20160822 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126740081 | 12674008 | 1 | PS | INDAPAMIDE. | INDAPAMIDE | 1 | DAILY. TAKEN FOR 3/4 DAYS ONLY. | Y | U | 74461 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126740081 | 12674008 | 1 | Hypertension |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126740081 | 12674008 | HO |
| 126740081 | 12674008 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126740081 | 12674008 | Balance disorder | |
| 126740081 | 12674008 | Confusional state | |
| 126740081 | 12674008 | Feeling abnormal | |
| 126740081 | 12674008 | Headache | |
| 126740081 | 12674008 | Hyponatraemia | |
| 126740081 | 12674008 | Syncope | |
| 126740081 | 12674008 | 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 |
|---|---|---|---|---|---|---|
| 126740081 | 12674008 | 1 | 201605 | 201605 | 0 |