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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 81822243 | 8182224 | 3 | F | 20110807 | 20121024 | 20111014 | 20121029 | EXP | CA-ROCHE-796947 | ROCHE | 62.87 | YR | F | Y | 77.18000 | KG | 20121030 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 81822243 | 8182224 | 1 | PS | Rituximab | 1 | INTRAVENOUS | D | UNKNOWN | 103705 | 1000 | MG | ||||||||
| 81822243 | 8182224 | 2 | C | MEDROL | 1 | D | 0 | ||||||||||||
| 81822243 | 8182224 | 3 | C | ADALAT | 1 | D | 0 | ||||||||||||
| 81822243 | 8182224 | 4 | C | INSULIN | 1 | D | 0 | ||||||||||||
| 81822243 | 8182224 | 5 | C | PREVACID | 1 | D | 0 | ||||||||||||
| 81822243 | 8182224 | 6 | C | SEPTRA DS | 1 | UNKNOWN | DRUG NAME MENTIONED AS CEPTRA DS, THERAPY DATES ; FOR 2 YEARS | D | 0 | ||||||||||
| 81822243 | 8182224 | 7 | C | COZAAR | 1 | D | 0 | ||||||||||||
| 81822243 | 8182224 | 8 | C | CALTRATE | 1 | D | 0 | ||||||||||||
| 81822243 | 8182224 | 9 | C | FOLIC ACID | 1 | D | 0 | ||||||||||||
| 81822243 | 8182224 | 10 | C | VITAMIN D3-5 | 2 | D | 0 | ||||||||||||
| 81822243 | 8182224 | 11 | C | CRESTOR | 1 | D | 0 | ||||||||||||
| 81822243 | 8182224 | 12 | C | MORPHINE | 1 | D | 0 | ||||||||||||
| 81822243 | 8182224 | 13 | C | OXYCOCET | 1 | D | 0 | ||||||||||||
| 81822243 | 8182224 | 14 | C | METRONIDAZOLE | 1 | UNKNOWN | DOSE : 14 PILLS | D | 0 | ||||||||||
| 81822243 | 8182224 | 15 | C | DIPHENHYDRAMINE HYDROCHLORIDE | 1 | ORAL | D | 0 | |||||||||||
| 81822243 | 8182224 | 16 | C | ACETAMINOFEN | 1 | ORAL | D | 0 | |||||||||||
| 81822243 | 8182224 | 17 | C | METHOTREXATE | 1 | D | 0 | ||||||||||||
| 81822243 | 8182224 | 18 | C | METHYLPREDNISOLONE | 1 | INTRAVENOUS | D | 0 | |||||||||||
| 81822243 | 8182224 | 19 | C | HUMULIN | 1 | D | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 81822243 | 8182224 | 1 | Rheumatoid arthritis |
| 81822243 | 8182224 | 3 | Blood pressure |
| 81822243 | 8182224 | 7 | Blood pressure |
| 81822243 | 8182224 | 12 | Pain |
| 81822243 | 8182224 | 13 | Pain |
| 81822243 | 8182224 | 14 | Antibiotic therapy |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 81822243 | 8182224 | OT |
| 81822243 | 8182224 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 81822243 | 8182224 | Angina pectoris | |
| 81822243 | 8182224 | Enteritis infectious | |
| 81822243 | 8182224 | Intestinal obstruction |
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 |
|---|---|---|---|---|---|---|
| 81822243 | 8182224 | 1 | 20091126 | 20100729 | 0 | |
| 81822243 | 8182224 | 18 | 20100729 | 0 |