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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125428751 | 12542875 | 1 | I | 20160630 | 20160710 | 20160710 | EXP | GB-DEXPHARM-20161297 | DEXCEL | 74.00 | YR | E | M | Y | 0.00000 | 20160710 | OT | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125428751 | 12542875 | 1 | PS | INDAPAMIDE. | INDAPAMIDE | 1 | Oral | DAILY DOSE: 2.5 MG MILLGRAM(S) EVERY DAYS | Y | U | 0 | 2.5 | MG | QD | |||||
125428751 | 12542875 | 2 | SS | OMEPRAZOLE. | OMEPRAZOLE | 1 | Oral | DAILY DOSE: 20 MG MILLGRAM(S) EVERY DAYS | Y | U | 0 | 20 | MG | QD | |||||
125428751 | 12542875 | 3 | C | CLOPIDOGREL | CLOPIDOGREL BISULFATE | 1 | 0 | ||||||||||||
125428751 | 12542875 | 4 | C | QUININE | QUININE | 1 | 0 | ||||||||||||
125428751 | 12542875 | 5 | C | SIMVASTATIN. | SIMVASTATIN | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125428751 | 12542875 | 1 | Hypertension |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125428751 | 12542875 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125428751 | 12542875 | Circulatory collapse | |
125428751 | 12542875 | Drug interaction | |
125428751 | 12542875 | Hypomagnesaemia | |
125428751 | 12542875 | Hyponatraemia |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |