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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127830951 | 12783095 | 1 | I | 20160914 | 20160927 | 20160927 | EXP | US-SUN PHARMACEUTICAL INDUSTRIES LTD-2016US-124743 | RANBAXY | 20.00 | YR | M | Y | 0.00000 | 20160927 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127830951 | 12783095 | 1 | PS | Loperamide | LOPERAMIDE | 1 | Unknown | 288 MG, DAILY (HIGH DOSES, 2 BOTTLES OF 2MG TABLETS) | Y | 74091 | 288 | MG | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127830951 | 12783095 | 1 | Drug withdrawal syndrome |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127830951 | 12783095 | LT |
| 127830951 | 12783095 | HO |
| 127830951 | 12783095 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127830951 | 12783095 | Congestive cardiomyopathy | |
| 127830951 | 12783095 | Drug abuse | |
| 127830951 | 12783095 | Syncope | |
| 127830951 | 12783095 | Torsade de pointes | |
| 127830951 | 12783095 | Ventricular arrhythmia |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |