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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123669294 | 12366929 | 4 | F | 201604 | 20160629 | 20160513 | 20160701 | EXP | DE-GILEAD-2016-0213441 | GILEAD | 0.00 | E | M | Y | 98.00000 | KG | 20160701 | MD | DE | DE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123669294 | 12366929 | 1 | PS | IDELALISIB | IDELALISIB | 1 | Oral | 300 MG, QD | Y | 205858 | 300 | MG | TABLET | QD | |||||
| 123669294 | 12366929 | 2 | SS | IDELALISIB | IDELALISIB | 1 | Oral | UNK | Y | 205858 | TABLET | ||||||||
| 123669294 | 12366929 | 3 | SS | MARCUMAR | PHENPROCOUMON | 1 | Unknown | U | 0 | ||||||||||
| 123669294 | 12366929 | 4 | C | MABTHERA | RITUXIMAB | 1 | Unknown | UNK | 0 | ||||||||||
| 123669294 | 12366929 | 5 | C | MABTHERA | RITUXIMAB | 1 | Unknown | UNK | 0 | ||||||||||
| 123669294 | 12366929 | 6 | C | RAMIPRIL. | RAMIPRIL | 1 | 0 | ||||||||||||
| 123669294 | 12366929 | 7 | C | FUROSEMIDE. | FUROSEMIDE | 1 | 0 | ||||||||||||
| 123669294 | 12366929 | 8 | C | ASPIRIN. | ASPIRIN | 1 | 0 | ||||||||||||
| 123669294 | 12366929 | 9 | C | OPIPRAMOL | OPIPRAMOL | 1 | 0 | ||||||||||||
| 123669294 | 12366929 | 10 | C | BISOPROLOL | BISOPROLOL | 1 | 0 | ||||||||||||
| 123669294 | 12366929 | 11 | C | BERODUAL | FENOTEROL HYDROBROMIDEIPRATROPIUM BROMIDE | 1 | UNK | 0 | |||||||||||
| 123669294 | 12366929 | 12 | C | ULTIBRO BREEZHALER | GLYCOPYRRONIUMINDACATEROL | 1 | UNK | 0 | |||||||||||
| 123669294 | 12366929 | 13 | C | PHENPROCOUMON | PHENPROCOUMON | 1 | UNK | 0 | |||||||||||
| 123669294 | 12366929 | 14 | C | NEBIVOLOL. | NEBIVOLOL | 1 | UNK | 0 | |||||||||||
| 123669294 | 12366929 | 15 | C | IBUPROFEN. | IBUPROFEN | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 123669294 | 12366929 | 1 | Product used for unknown indication |
| 123669294 | 12366929 | 3 | Product used for unknown indication |
| 123669294 | 12366929 | 11 | Chronic obstructive pulmonary disease |
| 123669294 | 12366929 | 12 | Chronic obstructive pulmonary disease |
| 123669294 | 12366929 | 13 | Atrial fibrillation |
| 123669294 | 12366929 | 14 | Cardiac failure |
| 123669294 | 12366929 | 15 | Osteoarthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 123669294 | 12366929 | HO |
| 123669294 | 12366929 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123669294 | 12366929 | Hepatotoxicity | |
| 123669294 | 12366929 | Overdose |
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 |
|---|---|---|---|---|---|---|
| 123669294 | 12366929 | 1 | 20160307 | 20160412 | 0 | |
| 123669294 | 12366929 | 2 | 20160513 | 0 | ||
| 123669294 | 12366929 | 4 | 20160307 | 20160307 | 0 | |
| 123669294 | 12366929 | 5 | 20160321 | 0 |