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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127764171 | 12776417 | 1 | I | 20160908 | 20160907 | 20160923 | 20160923 | EXP | US-ABBVIE-16P-163-1725921-00 | ABBVIE | 59.45 | YR | F | Y | 0.00000 | 20160923 | CN | COUNTRY NOT SPECIFIED | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127764171 | 12776417 | 1 | PS | VIEKIRA PAK | DASABUVIROMBITASVIRPARITAPREVIRRITONAVIR | 1 | Oral | N | UNKNOWN | 206619 | TABLET | ||||||||
127764171 | 12776417 | 2 | SS | VIEKIRA PAK | DASABUVIROMBITASVIRPARITAPREVIRRITONAVIR | 1 | N | UNKNOWN | 206619 | ||||||||||
127764171 | 12776417 | 3 | SS | RIBASPHERE | RIBAVIRIN | 1 | Oral | N | 0 | ||||||||||
127764171 | 12776417 | 4 | SS | RIBASPHERE | RIBAVIRIN | 1 | N | 0 | |||||||||||
127764171 | 12776417 | 5 | C | ALPRAZOLAM. | ALPRAZOLAM | 1 | 0 | ||||||||||||
127764171 | 12776417 | 6 | C | ASPIRIN. | ASPIRIN | 1 | 0 | ||||||||||||
127764171 | 12776417 | 7 | C | METHADONE | METHADONE HYDROCHLORIDE | 1 | 0 | ||||||||||||
127764171 | 12776417 | 8 | C | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127764171 | 12776417 | 1 | Chronic hepatitis C |
127764171 | 12776417 | 2 | Hepatic cirrhosis |
127764171 | 12776417 | 3 | Chronic hepatitis C |
127764171 | 12776417 | 4 | Hepatic cirrhosis |
127764171 | 12776417 | 5 | Product used for unknown indication |
127764171 | 12776417 | 6 | Product used for unknown indication |
127764171 | 12776417 | 7 | Product used for unknown indication |
127764171 | 12776417 | 8 | Diabetes mellitus |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127764171 | 12776417 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127764171 | 12776417 | Anaemia | |
127764171 | 12776417 | Blood pressure decreased | |
127764171 | 12776417 | Haematochezia |
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 |
---|---|---|---|---|---|---|
127764171 | 12776417 | 1 | 201608 | 20160908 | 0 | |
127764171 | 12776417 | 3 | 201608 | 20160908 | 0 |