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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125582361 | 12558236 | 1 | I | 20160705 | 20160714 | 20160714 | EXP | PHHY2016GB093003 | SANDOZ | 77.00 | YR | F | Y | 0.00000 | 20160714 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125582361 | 12558236 | 1 | PS | RAMIPRIL. | RAMIPRIL | 1 | Unknown | 77514 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125582361 | 12558236 | 1 | Hypertension |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125582361 | 12558236 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125582361 | 12558236 | Arthralgia | |
125582361 | 12558236 | Balance disorder | |
125582361 | 12558236 | Condition aggravated | |
125582361 | 12558236 | Dizziness | |
125582361 | 12558236 | Fall | |
125582361 | 12558236 | Head injury | |
125582361 | 12558236 | Insomnia | |
125582361 | 12558236 | Myalgia | |
125582361 | 12558236 | Sinusitis | |
125582361 | 12558236 | Sleep disorder | |
125582361 | 12558236 | Syncope | |
125582361 | 12558236 | Urine output increased |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |