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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125587451 | 12558745 | 1 | I | 20160616 | 20160715 | 20160715 | PER | US-JNJFOC-20160616488 | JANSSEN | 56.00 | YR | A | F | Y | 77.11000 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125587451 | 12558745 | 1 | PS | IMODIUM | LOPERAMIDE HYDROCHLORIDE | 1 | Oral | U | U | 19860 | CAPLET | ||||||||
| 125587451 | 12558745 | 2 | SS | IMODIUM | LOPERAMIDE HYDROCHLORIDE | 1 | Oral | DOSE: ONE CAPLET | U | U | 19860 | CAPLET | |||||||
| 125587451 | 12558745 | 3 | C | ZOLOFT | SERTRALINE HYDROCHLORIDE | 1 | Unknown | SINCE 12 YEARS | 0 | 50 | MG | UNSPECIFIED | QD | ||||||
| 125587451 | 12558745 | 4 | C | CLONAZEPAM. | CLONAZEPAM | 1 | Unknown | SINCE 12 YEARS | 0 | .25 | MG | UNSPECIFIED | BID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125587451 | 12558745 | 2 | Diarrhoea |
| 125587451 | 12558745 | 3 | Anxiety |
| 125587451 | 12558745 | 4 | Anxiety |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125587451 | 12558745 | Abdominal discomfort | |
| 125587451 | 12558745 | Off label use | |
| 125587451 | 12558745 | 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 |