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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124963452 | 12496345 | 2 | F | 20160614 | 20160624 | 20160715 | PER | US-JNJFOC-20160521964 | JANSSEN | 63.00 | YR | A | F | Y | 102.06000 | KG | 20160715 | CN | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124963452 | 12496345 | 1 | PS | IMODIUM MULTI-SYMPTOM RELIEF | DIMETHICONELOPERAMIDE HYDROCHLORIDE | 1 | Oral | N | DMF012 | 21140 | TABLET | ||||||||
| 124963452 | 12496345 | 2 | SS | IMODIUM MULTI-SYMPTOM RELIEF | DIMETHICONELOPERAMIDE HYDROCHLORIDE | 1 | Oral | N | DMF012 | 21140 | TABLET | ||||||||
| 124963452 | 12496345 | 3 | C | KAOPECTATE REGULAR STRENGTH CHERRY FLAVOR | BISMUTH SUBSALICYLATE | 1 | Unknown | 0 | UNSPECIFIED |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124963452 | 12496345 | 2 | Irritable bowel syndrome |
| 124963452 | 12496345 | 3 | Diarrhoea |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124963452 | 12496345 | Expired product administered | |
| 124963452 | 12496345 | Off label use | |
| 124963452 | 12496345 | Product use issue |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |