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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127133621 | 12713362 | 1 | I | 201512 | 20160512 | 20160902 | 20160902 | PER | US-ZYDUS-011150 | ZYDUS PHARM | 45.00 | YR | M | Y | 0.00000 | 20160902 | CN | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127133621 | 12713362 | 1 | PS | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Oral | Y | N | UNKNOWN | 78226 | 5 | MG | TABLET | |||||
| 127133621 | 12713362 | 2 | C | CANDESARTAN | CANDESARTAN | 1 | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127133621 | 12713362 | 1 | Hypertension |
| 127133621 | 12713362 | 2 | Hypertension |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127133621 | 12713362 | Drug ineffective | Drug ineffective |
| 127133621 | 12713362 | Fatigue | Fatigue |
| 127133621 | 12713362 | Headache | Headache |
| 127133621 | 12713362 | Photophobia | Photophobia |
| 127133621 | 12713362 | Tinnitus | Tinnitus |
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 |
|---|---|---|---|---|---|---|
| 127133621 | 12713362 | 1 | 201512 | 20151215 | 0 |