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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 97372199 | 9737219 | 9 | F | 201311 | 20160822 | 20131206 | 20160824 | EXP | CA-ROCHE-1312840 | ROCHE | 61.66 | YR | F | Y | 123.50000 | KG | 20160824 | OT | CA | CA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 97372199 | 9737219 | 1 | PS | RITUXAN | RITUXIMAB | 1 | Intravenous (not otherwise specified) | DOSE FREQUENCY: DAY 1 AND 15.?LAST DOSE OF RITUXAN: 14/JAN/2015 | Y | 103705 | 1000 | MG | SOLUTION FOR INFUSION | ||||||
| 97372199 | 9737219 | 2 | SS | ARTHROTEC | DICLOFENAC SODIUMMISOPROSTOL | 1 | Unknown | 0 | |||||||||||
| 97372199 | 9737219 | 3 | SS | BISOPROLOL | BISOPROLOL | 1 | Unknown | 0 | |||||||||||
| 97372199 | 9737219 | 4 | C | METHYLPREDNISOLONE. | METHYLPREDNISOLONE | 1 | Intravenous (not otherwise specified) | 0 | 100 | MG | |||||||||
| 97372199 | 9737219 | 5 | C | METHOTREXATE. | METHOTREXATE | 1 | 0 | ||||||||||||
| 97372199 | 9737219 | 6 | C | ACETAMINOPHEN. | ACETAMINOPHEN | 1 | Oral | 0 | 1000 | MG | |||||||||
| 97372199 | 9737219 | 7 | C | DIPHENHYDRAMINE HCL | DIPHENHYDRAMINE HYDROCHLORIDE | 1 | Oral | 0 | 50 | MG | |||||||||
| 97372199 | 9737219 | 8 | C | ACETYLSALICYLIC ACID | ASPIRIN | 1 | Unknown | 0 | 81 | MG | |||||||||
| 97372199 | 9737219 | 9 | C | TYLENOL EXTRA STRENGTH | ACETAMINOPHEN | 1 | 0 | ||||||||||||
| 97372199 | 9737219 | 10 | C | DIDROCAL | CALCIUM CARBONATEETIDRONATE DISODIUM | 1 | Unknown | 0 | |||||||||||
| 97372199 | 9737219 | 11 | C | PREDNISONE. | PREDNISONE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 97372199 | 9737219 | 1 | Rheumatoid arthritis |
| 97372199 | 9737219 | 2 | Product used for unknown indication |
| 97372199 | 9737219 | 3 | Product used for unknown indication |
| 97372199 | 9737219 | 4 | Premedication |
| 97372199 | 9737219 | 6 | Premedication |
| 97372199 | 9737219 | 7 | Premedication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 97372199 | 9737219 | OT |
| 97372199 | 9737219 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 97372199 | 9737219 | Atrial fibrillation | |
| 97372199 | 9737219 | Blood pressure diastolic decreased | |
| 97372199 | 9737219 | Blood pressure fluctuation | |
| 97372199 | 9737219 | Dementia | |
| 97372199 | 9737219 | Feeling abnormal | |
| 97372199 | 9737219 | Loss of consciousness | |
| 97372199 | 9737219 | Mood swings | |
| 97372199 | 9737219 | Stress | |
| 97372199 | 9737219 | Weight increased |
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 |
|---|---|---|---|---|---|---|
| 97372199 | 9737219 | 1 | 20120525 | 0 | ||
| 97372199 | 9737219 | 2 | 2013 | 0 | ||
| 97372199 | 9737219 | 4 | 20120525 | 0 | ||
| 97372199 | 9737219 | 6 | 20120525 | 0 | ||
| 97372199 | 9737219 | 7 | 20120525 | 0 | ||
| 97372199 | 9737219 | 10 | 2013 | 0 |