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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126532111 | 12653211 | 1 | I | 201603 | 20160321 | 20160815 | 20160815 | PER | US-ENDO PHARMACEUTICALS INC.-2016-002266 | ENDO | 74.00 | YR | M | Y | 87.62000 | KG | 20160815 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126532111 | 12653211 | 1 | PS | LACTULOSE ORAL SOLUTION | LACTULOSE | 1 | Oral | 3/4 TABLESPOON ONCE DAILY | U | UNKNOWN | 75993 | SOLUTION | |||||||
| 126532111 | 12653211 | 2 | SS | LACTULOSE ORAL SOLUTION | LACTULOSE | 1 | Oral | A LITTLE OVER 1 TABLESPOON ONCE DAILY | U | UNKNOWN | 75993 | SOLUTION |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126532111 | 12653211 | 1 | Constipation |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126532111 | 12653211 | Drug ineffective |
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 |
|---|---|---|---|---|---|---|
| 126532111 | 12653211 | 1 | 20160316 | 20160317 | 0 | |
| 126532111 | 12653211 | 2 | 20160317 | 0 |