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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126805461 | 12680546 | 1 | I | 20160128 | 20160701 | 20160824 | 20160824 | EXP | US-JNJFOC-20160704396 | PHARMACYCLICS | 65.20 | YR | A | F | Y | 50.00000 | KG | 20160824 | OT | US | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126805461 | 12680546 | 1 | PS | IMBRUVICA | IBRUTINIB | 1 | Oral | N | L0503308A1 | 205552 | 420 | MG | CAPSULE | QD | |||||
| 126805461 | 12680546 | 2 | SS | COUMADIN | WARFARIN SODIUM | 1 | 1 MG (MONDAY WEDNESDAY AND FRIDAY) | 0 | 1 | MG | TABLET | TIW | |||||||
| 126805461 | 12680546 | 3 | C | FOLIC ACID. | FOLIC ACID | 1 | Oral | 0 | 1 | MG | TABLET | QD | |||||||
| 126805461 | 12680546 | 4 | C | ACYCLOVIR. | ACYCLOVIR | 1 | Oral | 400 MG QD (EVERY 8 HOURS) | 0 | 400 | MG | TABLET | QD | ||||||
| 126805461 | 12680546 | 5 | C | DEXILANT | DEXLANSOPRAZOLE | 1 | Oral | 0 | 60 | MG | CAPSULE | QD | |||||||
| 126805461 | 12680546 | 6 | C | METHYLPREDNISOLONE. | METHYLPREDNISOLONE | 1 | Oral | 0 | 10 | ML | BID | ||||||||
| 126805461 | 12680546 | 7 | C | PREDNISONE. | PREDNISONE | 1 | Oral | 0 | 10 | MG | TABLET | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126805461 | 12680546 | 1 | Diffuse large B-cell lymphoma |
| 126805461 | 12680546 | 2 | Pulmonary embolism |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126805461 | 12680546 | DE |
| 126805461 | 12680546 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126805461 | 12680546 | Acute kidney injury | |
| 126805461 | 12680546 | Hyponatraemia | |
| 126805461 | 12680546 | International normalised ratio increased | |
| 126805461 | 12680546 | Leukocytosis | |
| 126805461 | 12680546 | Off label use | |
| 126805461 | 12680546 | Pneumonia bacterial | |
| 126805461 | 12680546 | Product use issue | |
| 126805461 | 12680546 | Sepsis |
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 |
|---|---|---|---|---|---|---|
| 126805461 | 12680546 | 1 | 20160128 | 20160621 | 0 |