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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125609031 | 12560903 | 1 | I | 20160701 | 20160715 | 20160715 | EXP | US-SUN PHARMACEUTICAL INDUSTRIES LTD-2016US-120239 | RANBAXY | 33.00 | YR | M | Y | 0.00000 | 20160715 | OT | GB | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125609031 | 12560903 | 1 | PS | Loperamide | LOPERAMIDE | 1 | Unknown | 35 DF 2 MG TABLETS (70 MG), DAILY | U | U | 74091 | TABLET | |||||||
| 125609031 | 12560903 | 2 | SS | Loperamide | LOPERAMIDE | 1 | Unknown | 140 MG IN 7 HOURS (ON THE DAY OF ADMISSION) | U | U | 74091 | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125609031 | 12560903 | 1 | Drug withdrawal syndrome |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125609031 | 12560903 | OT |
| 125609031 | 12560903 | LT |
| 125609031 | 12560903 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125609031 | 12560903 | Drug abuse | |
| 125609031 | 12560903 | Electrocardiogram QT prolonged |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |