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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126705872 | 12670587 | 2 | F | 20160811 | 20160822 | 20160822 | EXP | GB-MHRA-ADR 23590668 | GB-CIPLA LTD.-2016GB17549 | CIPLA | 0.00 | Y | 0.00000 | 20160822 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126705872 | 12670587 | 1 | PS | RAMIPRIL. | RAMIPRIL | 1 | Unknown | UNK | U | U | 77004 | ||||||||
126705872 | 12670587 | 2 | SS | LOSARTAN. | LOSARTAN | 1 | Unknown | UNK | U | U | 0 | ||||||||
126705872 | 12670587 | 3 | SS | ADIZEM | DILTIAZEM HYDROCHLORIDE | 1 | Unknown | UNK | U | U | 0 | ||||||||
126705872 | 12670587 | 4 | C | Bendroflumethiazide | BENDROFLUMETHIAZIDE | 1 | Unknown | UNK | U | U | 0 |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126705872 | 12670587 | OT |
126705872 | 12670587 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126705872 | 12670587 | Aphonia | |
126705872 | 12670587 | Hypokalaemia | |
126705872 | 12670587 | Pneumonia | |
126705872 | 12670587 | Syncope |
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 |
---|---|---|---|---|---|---|
126705872 | 12670587 | 4 | 201607 | 0 |