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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125712471 | 12571247 | 1 | I | 20160705 | 20160719 | 20160719 | EXP | SE-TEVA-676260ISR | TEVA | 57.00 | YR | M | Y | 0.00000 | 20160719 | OT | SE | SE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125712471 | 12571247 | 1 | PS | IBUPROFEN. | IBUPROFEN | 1 | Unknown | U | 71145 | ||||||||||
| 125712471 | 12571247 | 2 | SS | PARACETAMOL | ACETAMINOPHEN | 1 | Unknown | U | 0 | ||||||||||
| 125712471 | 12571247 | 3 | SS | TARGINIQ ER | NALOXONE HYDROCHLORIDEOXYCODONE HYDROCHLORIDE | 1 | U | 0 | PROLONGED-RELEASE TABLET | ||||||||||
| 125712471 | 12571247 | 4 | SS | TRAMADOL. | TRAMADOL | 1 | U | 0 | |||||||||||
| 125712471 | 12571247 | 5 | SS | Zopiclone | ZOPICLONE | 1 | U | 0 | |||||||||||
| 125712471 | 12571247 | 6 | SS | amitriptyline | AMITRIPTYLINE | 1 | U | 0 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125712471 | 12571247 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125712471 | 12571247 | Agitation | |
| 125712471 | 12571247 | Fatigue | |
| 125712471 | 12571247 | Toxicity to various agents |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |