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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126518601 | 12651860 | 1 | I | 20160614 | 20160815 | 20160815 | PER | US-ASTRAZENECA-2016SE66122 | ASTRAZENECA | 60.00 | YR | F | Y | 104.30000 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126518601 | 12651860 | 1 | PS | MOVANTIK | NALOXEGOL OXALATE | 1 | Oral | 204760 | 25 | MG | TABLET | QD | |||||||
| 126518601 | 12651860 | 2 | SS | MOVANTIK | NALOXEGOL OXALATE | 1 | Oral | 25.0MG UNKNOWN | 204760 | 25 | MG | TABLET | |||||||
| 126518601 | 12651860 | 3 | SS | ATENOLOL. | ATENOLOL | 1 | Oral | 0 | 50 | MG | TABLET | QD | |||||||
| 126518601 | 12651860 | 4 | C | NABUMETONE. | NABUMETONE | 1 | Oral | 0 | 500 | MG | BID | ||||||||
| 126518601 | 12651860 | 5 | C | CHLORTHALIDONE. | CHLORTHALIDONE | 1 | Oral | 0 | 25 | MG | QD | ||||||||
| 126518601 | 12651860 | 6 | C | OXYCODONE | OXYCODONE | 1 | Oral | 0 | 15 | MG | TID | ||||||||
| 126518601 | 12651860 | 7 | C | OXYCODONE EXTENDED RELEASE | OXYCODONE | 1 | Oral | 20 MG, TWICE A DAY AS NEEDED | 0 | ||||||||||
| 126518601 | 12651860 | 8 | C | XANAX | ALPRAZOLAM | 1 | Oral | 1 G, THREE TIMES A DAY AS NEEDED | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126518601 | 12651860 | 1 | Constipation |
| 126518601 | 12651860 | 2 | Constipation |
| 126518601 | 12651860 | 3 | Blood pressure abnormal |
| 126518601 | 12651860 | 4 | Arthritis |
| 126518601 | 12651860 | 5 | Renal disorder |
| 126518601 | 12651860 | 6 | Pain |
| 126518601 | 12651860 | 7 | Pain |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126518601 | 12651860 | Intentional product misuse | |
| 126518601 | 12651860 | Nausea |
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 |
|---|---|---|---|---|---|---|
| 126518601 | 12651860 | 1 | 2016 | 2016 | 0 | |
| 126518601 | 12651860 | 2 | 2016 | 0 |