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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126846571 | 12684657 | 1 | I | 20160715 | 20160818 | 20160825 | 20160825 | EXP | PHHY2016IT115772 | SANDOZ | 41.00 | YR | F | Y | 0.00000 | 20160825 | CN | IT | IT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126846571 | 12684657 | 1 | PS | IBUPROFEN. | IBUPROFEN | 1 | Oral | 400 MG, UNK | U | 70733 | 400 | MG | |||||||
| 126846571 | 12684657 | 2 | SS | IMODIUM | LOPERAMIDE HYDROCHLORIDE | 1 | Oral | 2 MG, UNK | U | 0 | 2 | MG | CAPSULE | ||||||
| 126846571 | 12684657 | 3 | SS | MOTILIUM | DOMPERIDONE | 1 | Oral | 10 MG, UNK | U | 0 | 10 | MG | ORAL SUSPENSION |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126846571 | 12684657 | 1 | Pain |
| 126846571 | 12684657 | 2 | Pain |
| 126846571 | 12684657 | 3 | Pain |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126846571 | 12684657 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126846571 | 12684657 | Abdominal pain | |
| 126846571 | 12684657 | Intentional product misuse |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |