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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124794722 | 12479472 | 2 | F | 20160630 | 20160620 | 20160708 | EXP | ES-MLMSERVICE-20160608-0314075-1 | ES-STRIDES ARCOLAB LIMITED-2016SP007685 | STRIDES | 0.00 | Y | 0.00000 | 20160707 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124794722 | 12479472 | 1 | PS | IBUPROFEN. | IBUPROFEN | 1 | Oral | UNK | U | U | 0 | ||||||||
| 124794722 | 12479472 | 2 | SS | IBUPROFEN. | IBUPROFEN | 1 | Oral | 10 G, UNK | U | U | 0 | 10 | G |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124794722 | 12479472 | 1 | Back pain |
| 124794722 | 12479472 | 2 | Haemoptysis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124794722 | 12479472 | HO |
| 124794722 | 12479472 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124794722 | 12479472 | Acute kidney injury | |
| 124794722 | 12479472 | Anaemia | |
| 124794722 | 12479472 | Cough | |
| 124794722 | 12479472 | Diffuse alveolar damage | |
| 124794722 | 12479472 | Drug abuse |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |