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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124209862 | 12420986 | 2 | F | 20160719 | 20160531 | 20160727 | EXP | NZ-KADMON PHARMACEUTICALS, LLC-KAD201605-001963 | KADMON | 0.00 | F | Y | 0.00000 | 20160727 | MD | NZ | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124209862 | 12420986 | 1 | PS | RIBAVIRIN. | RIBAVIRIN | 1 | 76203 | ||||||||||||
| 124209862 | 12420986 | 2 | SS | VIEKIRA PAK | DASABUVIROMBITASVIRPARITAPREVIRRITONAVIR | 1 | Oral | TABLET | 0 | TABLET | |||||||||
| 124209862 | 12420986 | 3 | SS | TRAMADOL. | TRAMADOL | 1 | 0 | 50 | MG | BID | |||||||||
| 124209862 | 12420986 | 4 | C | Codeine | CODEINE | 1 | 0 | 15 | MG | TID | |||||||||
| 124209862 | 12420986 | 5 | C | Nortriptyline | NORTRIPTYLINE | 1 | 0 | 25 | MG | ||||||||||
| 124209862 | 12420986 | 6 | C | PAROXETINE. | PAROXETINE | 1 | 0 | 20 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124209862 | 12420986 | 1 | Hepatitis C |
| 124209862 | 12420986 | 2 | Hepatitis C |
| 124209862 | 12420986 | 3 | Back pain |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124209862 | 12420986 | OT |
| 124209862 | 12420986 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124209862 | 12420986 | Adverse drug reaction | |
| 124209862 | 12420986 | Blood bilirubin increased | |
| 124209862 | 12420986 | Drug interaction | |
| 124209862 | 12420986 | Gastrointestinal disorder | |
| 124209862 | 12420986 | Hallucination | |
| 124209862 | 12420986 | Hepatic failure | |
| 124209862 | 12420986 | Hypophagia | |
| 124209862 | 12420986 | Insomnia | |
| 124209862 | 12420986 | International normalised ratio increased | |
| 124209862 | 12420986 | Nausea | |
| 124209862 | 12420986 | 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 |
|---|---|---|---|---|---|---|
| 124209862 | 12420986 | 1 | 2016 | 2016 | 0 | |
| 124209862 | 12420986 | 2 | 20160426 | 20160516 | 0 |