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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124876332 | 12487633 | 2 | F | 20160701 | 20160622 | 20160715 | EXP | ES-SUN PHARMACEUTICAL INDUSTRIES LTD-2016R1-118776 | RANBAXY | 49.00 | YR | M | Y | 0.00000 | 20160715 | OT | GB | ES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124876332 | 12487633 | 1 | PS | IBUPROFEN. | IBUPROFEN | 1 | Oral | APPROXIMATELY 10 G A DAY | U | 71214 | |||||||||
| 124876332 | 12487633 | 2 | SS | IBUPROFEN. | IBUPROFEN | 1 | U | 71214 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124876332 | 12487633 | 1 | Back pain |
| 124876332 | 12487633 | 2 | Haemoptysis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124876332 | 12487633 | OT |
| 124876332 | 12487633 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124876332 | 12487633 | Acute kidney injury | |
| 124876332 | 12487633 | Diffuse alveolar damage | |
| 124876332 | 12487633 | Drug abuse |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |