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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 119036392 | 11903639 | 2 | F | 20160319 | 20160108 | 20160805 | PER | US-ABBVIE-15P-163-1505084-00 | ABBVIE | 0.00 | F | Y | 0.00000 | 20160805 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 119036392 | 11903639 | 1 | PS | VIEKIRA PAK | DASABUVIROMBITASVIRPARITAPREVIRRITONAVIR | 1 | Oral | UNKNOWN | 206619 | ||||||||||
| 119036392 | 11903639 | 2 | SS | RIBAVIRIN. | RIBAVIRIN | 1 | Oral | UNKNOWN | 0 | ||||||||||
| 119036392 | 11903639 | 3 | C | BACLOFEN. | BACLOFEN | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 119036392 | 11903639 | 1 | Hepatitis C |
| 119036392 | 11903639 | 2 | Hepatitis C |
| 119036392 | 11903639 | 3 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 119036392 | 11903639 | Fatigue | |
| 119036392 | 11903639 | Feeling abnormal | |
| 119036392 | 11903639 | Malaise | |
| 119036392 | 11903639 | Nausea | |
| 119036392 | 11903639 | Transfusion | |
| 119036392 | 11903639 | Tremor | |
| 119036392 | 11903639 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |