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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127001891 | 12700189 | 1 | I | 20160805 | 20160825 | 20160830 | 20160830 | EXP | RO-ABBVIE-16P-135-1713366-00 | ABBVIE | 70.80 | YR | F | Y | 0.00000 | 20160830 | MD | COUNTRY NOT SPECIFIED | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127001891 | 12700189 | 1 | PS | VIEKIRAX | OMBITASVIRPARITAPREVIRRITONAVIR | 1 | Oral | Y | Y | UNKNOWN | 206619 | TABLET | |||||||
| 127001891 | 12700189 | 2 | SS | VIEKIRAX | OMBITASVIRPARITAPREVIRRITONAVIR | 1 | Oral | Y | Y | UNKNOWN | 206619 | TABLET | |||||||
| 127001891 | 12700189 | 3 | SS | EXVIERA | DASABUVIR | 1 | Oral | Y | Y | UNKNOWN | 206619 | TABLET | |||||||
| 127001891 | 12700189 | 4 | SS | EXVIERA | DASABUVIR | 1 | Oral | Y | Y | UNKNOWN | 206619 | TABLET | |||||||
| 127001891 | 12700189 | 5 | SS | REBETOL | RIBAVIRIN | 1 | Oral | Y | Y | 0 | 200 | MG | TABLET | ||||||
| 127001891 | 12700189 | 6 | SS | REBETOL | RIBAVIRIN | 1 | Oral | Y | Y | 0 | TABLET | ||||||||
| 127001891 | 12700189 | 7 | C | NIFEDIPIN | NIFEDIPINE | 1 | Oral | 0 | |||||||||||
| 127001891 | 12700189 | 8 | C | ACCUPRO | QUINAPRIL HYDROCHLORIDE | 1 | Oral | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127001891 | 12700189 | 1 | Hepatitis C |
| 127001891 | 12700189 | 3 | Hepatitis C |
| 127001891 | 12700189 | 5 | Hepatitis C |
| 127001891 | 12700189 | 7 | Product used for unknown indication |
| 127001891 | 12700189 | 8 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127001891 | 12700189 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127001891 | 12700189 | Asthenia | Asthenia |
| 127001891 | 12700189 | Dizziness | Dizziness |
| 127001891 | 12700189 | Headache | Headache |
| 127001891 | 12700189 | Nausea | Nausea |
| 127001891 | 12700189 | Pruritus | |
| 127001891 | 12700189 | Tremor | Tremor |
| 127001891 | 12700189 | Vomiting | Vomiting |
| 127001891 | 12700189 | Wheezing | Wheezing |
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 |
|---|---|---|---|---|---|---|
| 127001891 | 12700189 | 1 | 20160805 | 20160817 | 0 | |
| 127001891 | 12700189 | 2 | 20160820 | 20160820 | 0 | |
| 127001891 | 12700189 | 3 | 20160805 | 20160817 | 0 | |
| 127001891 | 12700189 | 4 | 20160820 | 20160820 | 0 | |
| 127001891 | 12700189 | 5 | 20160805 | 20160817 | 0 | |
| 127001891 | 12700189 | 6 | 20160820 | 20160820 | 0 |