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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126436843 | 12643684 | 3 | F | 20160727 | 20160825 | 20160811 | 20160901 | EXP | JP-ABBVIE-16P-087-1694782-00 | ABBVIE | 74.00 | YR | M | Y | 0.00000 | 20160901 | PH | JP | JP |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126436843 | 12643684 | 1 | PS | VIEKIRAX | OMBITASVIRPARITAPREVIRRITONAVIR | 1 | Oral | UNKNOWN | 207931 | TABLET | |||||||||
| 126436843 | 12643684 | 2 | SS | RABEPRAZOLE SODIUM. | RABEPRAZOLE SODIUM | 1 | Oral | U | 0 | ||||||||||
| 126436843 | 12643684 | 3 | C | CEFDINIR. | CEFDINIR | 1 | Oral | 0 | |||||||||||
| 126436843 | 12643684 | 4 | C | CLARITHROMYCIN. | CLARITHROMYCIN | 1 | Oral | 0 | |||||||||||
| 126436843 | 12643684 | 5 | C | BUDESONIDE/FORMOTEROL FUMARATE HYDRATE | 2 | Respiratory (inhalation) | 0 | INHALATION POWDER |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126436843 | 12643684 | 1 | Hepatitis C |
| 126436843 | 12643684 | 2 | Product used for unknown indication |
| 126436843 | 12643684 | 3 | Product used for unknown indication |
| 126436843 | 12643684 | 4 | Product used for unknown indication |
| 126436843 | 12643684 | 5 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126436843 | 12643684 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126436843 | 12643684 | Cerebral haemorrhage | |
| 126436843 | 12643684 | Epistaxis | |
| 126436843 | 12643684 | Platelet count decreased |
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 |
|---|---|---|---|---|---|---|
| 126436843 | 12643684 | 1 | 20160413 | 20160706 | 0 | |
| 126436843 | 12643684 | 2 | 201607 | 0 |