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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124543572 | 12454357 | 2 | F | 20160616 | 20160610 | 20160701 | EXP | US-SUN PHARMACEUTICAL INDUSTRIES LTD-2016US-118117 | RANBAXY | 28.00 | YR | F | Y | 0.00000 | 20160701 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124543572 | 12454357 | 1 | PS | Loperamide | LOPERAMIDE | 1 | Oral | 400-600 MG; IN THE FORM OF 2 MG TABLETS | Y | 74091 | TABLET | ||||||||
| 124543572 | 12454357 | 2 | I | Loperamide | LOPERAMIDE | 1 | Oral | 100 DF, DAILY | Y | 74091 | 100 | DF | TABLET | ||||||
| 124543572 | 12454357 | 3 | I | Cimetidine | CIMETIDINE | 1 | Oral | IN THE FORM OF 200 MG TABLETS | Y | 0 | 2000 | MG | TABLET | ||||||
| 124543572 | 12454357 | 4 | I | CIMETIDINE | CIMETIDINE | 1 | Oral | 10 DF, DAILY | Y | 0 | 10 | DF | TABLET | ||||||
| 124543572 | 12454357 | 5 | C | GABAPENTIN. | GABAPENTIN | 1 | Unknown | UNK | U | 0 | |||||||||
| 124543572 | 12454357 | 6 | C | MORPHINE | MORPHINE | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124543572 | 12454357 | 1 | Drug withdrawal syndrome |
| 124543572 | 12454357 | 2 | Drug withdrawal syndrome |
| 124543572 | 12454357 | 3 | Drug withdrawal syndrome |
| 124543572 | 12454357 | 4 | Drug withdrawal syndrome |
| 124543572 | 12454357 | 5 | Drug withdrawal syndrome |
| 124543572 | 12454357 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124543572 | 12454357 | HO |
| 124543572 | 12454357 | LT |
| 124543572 | 12454357 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124543572 | 12454357 | Arrhythmia | |
| 124543572 | 12454357 | Atrioventricular block first degree | |
| 124543572 | 12454357 | Cardiac murmur | |
| 124543572 | 12454357 | Drug abuse | |
| 124543572 | 12454357 | Drug interaction | |
| 124543572 | 12454357 | Electrocardiogram QRS complex prolonged | |
| 124543572 | 12454357 | Electrocardiogram QT prolonged | |
| 124543572 | 12454357 | Electrocardiogram T wave amplitude decreased | |
| 124543572 | 12454357 | Electrocardiogram T wave inversion | |
| 124543572 | 12454357 | Myoclonus | |
| 124543572 | 12454357 | Overdose | |
| 124543572 | 12454357 | QRS axis abnormal | |
| 124543572 | 12454357 | Self-medication | |
| 124543572 | 12454357 | Sinus bradycardia | |
| 124543572 | 12454357 | Syncope | |
| 124543572 | 12454357 | Torsade de pointes |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |