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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125012742 | 12501274 | 2 | F | 201503 | 20160711 | 20160627 | 20160715 | EXP | US-PURDUE PHARMA-USA-2016-0131023 | PURDUE | 65.28 | YR | F | Y | 136.50000 | KG | 20160715 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125012742 | 12501274 | 1 | PS | Oxycodone HCl CR Tablets (similar to NDA 22-272) | OXYCODONE HYDROCHLORIDE | 1 | Oral | U | U | UNKNOWN | 22272 | PROLONGED-RELEASE TABLET | |||||||
| 125012742 | 12501274 | 2 | SS | HYDROCODONE | HYDROCODONE | 1 | Oral | U | U | UNKNOWN | 0 | ||||||||
| 125012742 | 12501274 | 3 | SS | Oxycodone/ Acetaminophen Tablets | ACETAMINOPHENOXYCODONE HYDROCHLORIDE | 1 | Oral | 7.5/325, UNK | N | UNKNOWN | 0 | TABLET | |||||||
| 125012742 | 12501274 | 4 | C | HYDROCHLOROTHIAZIDE. | HYDROCHLOROTHIAZIDE | 1 | Unknown | 25 MG, UNK | U | UNKNOWN | 0 | 25 | MG | ||||||
| 125012742 | 12501274 | 5 | C | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | Unknown | 500 MG, UNK | U | UNKNOWN | 0 | 500 | MG | ||||||
| 125012742 | 12501274 | 6 | C | SIMVASTATIN. | SIMVASTATIN | 1 | Unknown | 20 MG, UNK | U | UNKNOWN | 0 | 20 | MG | ||||||
| 125012742 | 12501274 | 7 | C | CLONIDINE. | CLONIDINE | 1 | 0.1 MG, UNK | U | UNKNOWN | 0 | .1 | MG | |||||||
| 125012742 | 12501274 | 8 | C | CLONIDINE. | CLONIDINE | 1 | Oral | 1 MG, UNK | U | UNKNOWN | 0 | 1 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125012742 | 12501274 | 1 | Osteoarthritis |
| 125012742 | 12501274 | 2 | Osteoarthritis |
| 125012742 | 12501274 | 3 | Osteoarthritis |
| 125012742 | 12501274 | 4 | Hypertension |
| 125012742 | 12501274 | 5 | Diabetes mellitus |
| 125012742 | 12501274 | 6 | Hypertension |
| 125012742 | 12501274 | 7 | Depression |
| 125012742 | 12501274 | 8 | Blood pressure measurement |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125012742 | 12501274 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125012742 | 12501274 | Abdominal distension | |
| 125012742 | 12501274 | Activities of daily living impaired | |
| 125012742 | 12501274 | Constipation | |
| 125012742 | 12501274 | Functional gastrointestinal disorder | |
| 125012742 | 12501274 | Incontinence | |
| 125012742 | 12501274 | Nausea | |
| 125012742 | 12501274 | Pain | |
| 125012742 | 12501274 | Swelling | |
| 125012742 | 12501274 | Vomiting |
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 |
|---|---|---|---|---|---|---|
| 125012742 | 12501274 | 3 | 201505 | 201509 | 0 | |
| 125012742 | 12501274 | 4 | 1980 | 0 | ||
| 125012742 | 12501274 | 5 | 2014 | 0 | ||
| 125012742 | 12501274 | 6 | 1990 | 0 | ||
| 125012742 | 12501274 | 7 | 2012 | 0 | ||
| 125012742 | 12501274 | 8 | 1990 | 0 |