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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124125463 | 12412546 | 3 | F | 20160719 | 20160527 | 20160721 | EXP | NZ-ABBVIE-16P-118-1636728-00 | ABBVIE | 0.00 | F | Y | 0.00000 | 20160721 | OT | COUNTRY NOT SPECIFIED | NZ |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124125463 | 12412546 | 1 | PS | VIEKIRA PAK | DASABUVIROMBITASVIRPARITAPREVIRRITONAVIR | 1 | Oral | Y | UNKNOWN | 206619 | TABLET | ||||||||
| 124125463 | 12412546 | 2 | SS | RIBAVIRIN. | RIBAVIRIN | 1 | Unknown | Y | UNKNOWN | 0 | |||||||||
| 124125463 | 12412546 | 3 | I | TRAMADOL. | TRAMADOL | 1 | Unknown | BD | Y | UNKNOWN | 0 | 50 | MG | ||||||
| 124125463 | 12412546 | 4 | C | CODEINE | CODEINE | 1 | TDS | 0 | 15 | MG | |||||||||
| 124125463 | 12412546 | 5 | C | NORTRIPTYLINE | NORTRIPTYLINE | 1 | NOCTE | 0 | 25 | MG | |||||||||
| 124125463 | 12412546 | 6 | C | PAROXETINE. | PAROXETINE | 1 | 0 | 20 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124125463 | 12412546 | 1 | Chronic hepatitis C |
| 124125463 | 12412546 | 2 | Chronic hepatitis C |
| 124125463 | 12412546 | 3 | Back pain |
| 124125463 | 12412546 | 4 | Product used for unknown indication |
| 124125463 | 12412546 | 5 | Product used for unknown indication |
| 124125463 | 12412546 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124125463 | 12412546 | OT |
| 124125463 | 12412546 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124125463 | 12412546 | Adverse drug reaction | |
| 124125463 | 12412546 | Blood bilirubin increased | |
| 124125463 | 12412546 | Drug interaction | |
| 124125463 | 12412546 | Gastrointestinal disorder | |
| 124125463 | 12412546 | Hallucination | |
| 124125463 | 12412546 | Hepatic failure | |
| 124125463 | 12412546 | Hypophagia | |
| 124125463 | 12412546 | Insomnia | |
| 124125463 | 12412546 | International normalised ratio increased | |
| 124125463 | 12412546 | Nausea | |
| 124125463 | 12412546 | Somnolence |
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 |
|---|---|---|---|---|---|---|
| 124125463 | 12412546 | 1 | 20160426 | 20160516 | 0 | |
| 124125463 | 12412546 | 2 | 2016 | 2016 | 0 |