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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125574611 | 12557461 | 1 | I | 20160614 | 20160622 | 20160714 | 20160714 | EXP | RO-KADMON PHARMACEUTICALS, LLC-KAD201607-002412 | KADMON | 58.82 | YR | F | Y | 0.00000 | 20160714 | CN | RO | RO |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125574611 | 12557461 | 1 | PS | RIBAVIRIN. | RIBAVIRIN | 1 | Oral | FILM-COATED TABLET, 2 IN THE MORNING AND 3 IN THE EVENING | Y | 1054936 | 77456 | FILM-COATED TABLET | |||||||
125574611 | 12557461 | 2 | SS | RIBAVIRIN. | RIBAVIRIN | 1 | Oral | Y | 1054936 | 77456 | |||||||||
125574611 | 12557461 | 3 | SS | Viekirax | OMBITASVIRPARITAPREVIRRITONAVIR | 1 | Oral | FILM-COATED TABLET | 1058724 | 0 | FILM-COATED TABLET | ||||||||
125574611 | 12557461 | 4 | SS | Viekirax | OMBITASVIRPARITAPREVIRRITONAVIR | 1 | 1058724 | 0 | |||||||||||
125574611 | 12557461 | 5 | SS | Exviera | DASABUVIR | 1 | Oral | FILM-COATED TABLET | 1059064 | 0 | FILM-COATED TABLET | ||||||||
125574611 | 12557461 | 6 | SS | Exviera | DASABUVIR | 1 | 1059064 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125574611 | 12557461 | 1 | Hepatitis C |
125574611 | 12557461 | 2 | Hepatic cirrhosis |
125574611 | 12557461 | 3 | Hepatitis C |
125574611 | 12557461 | 4 | Hepatic cirrhosis |
125574611 | 12557461 | 5 | Hepatitis C |
125574611 | 12557461 | 6 | Hepatic cirrhosis |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125574611 | 12557461 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125574611 | 12557461 | Chest pain | |
125574611 | 12557461 | Chills | |
125574611 | 12557461 | Dizziness | |
125574611 | 12557461 | Epistaxis | |
125574611 | 12557461 | Fatigue | |
125574611 | 12557461 | Gingival bleeding | |
125574611 | 12557461 | Nausea | |
125574611 | 12557461 | Parosmia | |
125574611 | 12557461 | Peripheral coldness | |
125574611 | 12557461 | Posture abnormal | |
125574611 | 12557461 | Pruritus | |
125574611 | 12557461 | Swelling | |
125574611 | 12557461 | Tinnitus | |
125574611 | 12557461 | Unevaluable event | |
125574611 | 12557461 | Vascular fragility |
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 |
---|---|---|---|---|---|---|
125574611 | 12557461 | 1 | 20160614 | 20160627 | 0 | |
125574611 | 12557461 | 2 | 20160628 | 0 | ||
125574611 | 12557461 | 3 | 20160614 | 0 | ||
125574611 | 12557461 | 5 | 20160614 | 0 |