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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125174593 | 12517459 | 3 | F | 20160729 | 20160630 | 20160812 | EXP | GR-SUN PHARMACEUTICAL INDUSTRIES LTD-2016R1-119230 | RANBAXY | 72.00 | YR | M | Y | 0.00000 | 20160812 | OT | GB | GR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125174593 | 12517459 | 1 | PS | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Unknown | Y | 77974 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125174593 | 12517459 | 1 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125174593 | 12517459 | HO |
| 125174593 | 12517459 | LT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125174593 | 12517459 | Anaemia | |
| 125174593 | 12517459 | Blood creatinine increased | |
| 125174593 | 12517459 | Drug level increased | |
| 125174593 | 12517459 | Hyperglycaemia | |
| 125174593 | 12517459 | Hypotension | |
| 125174593 | 12517459 | Overdose | |
| 125174593 | 12517459 | Shock | |
| 125174593 | 12517459 | Toxicity to various agents |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |