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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127302911 | 12730291 | 1 | I | 20160724 | 20160901 | 20160909 | 20160909 | EXP | CN-NAPPMUNDI-GBR-2016-0040346 | PURDUE | 62.00 | YR | M | Y | 68.00000 | KG | 20160908 | OT | CN | CN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127302911 | 12730291 | 1 | PS | MS CONTIN | MORPHINE SULFATE | 1 | Oral | 30 MG, Q12H | 180 | MG | 1304123 | 19516 | 30 | MG | PROLONGED-RELEASE TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127302911 | 12730291 | 1 | Abdominal pain upper |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127302911 | 12730291 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127302911 | 12730291 | Constipation | |
| 127302911 | 12730291 | Decreased appetite | |
| 127302911 | 12730291 | Hypophagia |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 127302911 | 12730291 | 1 | 20160722 | 20160726 | 0 |