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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125164982 | 12516498 | 2 | F | 20160630 | 20160630 | 20160713 | EXP | GB-AUROBINDO-AUR-APL-2016-08183 | AUROBINDO | 0.00 | Y | 0.00000 | 20160713 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125164982 | 12516498 | 1 | PS | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Oral | UNK | Y | U | 78021 | ||||||||
| 125164982 | 12516498 | 2 | SS | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Y | U | 78021 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125164982 | 12516498 | 1 | Hypertension |
| 125164982 | 12516498 | 2 | Hypertension |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125164982 | 12516498 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125164982 | 12516498 | Joint swelling | |
| 125164982 | 12516498 | Pain | |
| 125164982 | 12516498 | Peripheral swelling | |
| 125164982 | 12516498 | Skin ulcer |
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 |
|---|---|---|---|---|---|---|
| 125164982 | 12516498 | 1 | 20160428 | 20160505 | 0 |