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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 117477313 | 11747731 | 3 | F | 2015 | 20160707 | 20151117 | 20160720 | EXP | CA-PFIZER INC-2015389658 | PFIZER | 79.00 | YR | F | Y | 0.00000 | 20160720 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 117477313 | 11747731 | 1 | PS | SULFASALAZINE. | SULFASALAZINE | 1 | Oral | 1 G, 1X/DAY | 7073 | 1 | G | MODIFIED-RELEASE TABLET | QD | ||||||
| 117477313 | 11747731 | 2 | SS | ARAVA | LEFLUNOMIDE | 1 | Oral | 20 MG, 1X/DAY | 0 | 20 | MG | QD | |||||||
| 117477313 | 11747731 | 3 | SS | DURELA | TRAMADOL HYDROCHLORIDE | 1 | Oral | 100 MG, 1X/DAY AT BEDTIME | 0 | 100 | MG | QD | |||||||
| 117477313 | 11747731 | 4 | C | APO-FUROSEMIDE | FUROSEMIDE | 1 | 40 MG, UNK | 0 | 40 | MG | |||||||||
| 117477313 | 11747731 | 5 | C | ENABLEX | DARIFENACIN HYDROBROMIDE | 1 | 7.5 MG ER, UNK | 0 | 7.5 | MG | |||||||||
| 117477313 | 11747731 | 6 | C | AVA-IRBESARTAN | 2 | 300 MG, UNK | 0 | 300 | MG | ||||||||||
| 117477313 | 11747731 | 7 | C | CRESTOR | ROSUVASTATIN CALCIUM | 1 | 20 MG, UNK | 0 | 20 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 117477313 | 11747731 | 1 | Rheumatoid arthritis |
| 117477313 | 11747731 | 2 | Rheumatoid arthritis |
| 117477313 | 11747731 | 3 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 117477313 | 11747731 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 117477313 | 11747731 | Activities of daily living impaired | |
| 117477313 | 11747731 | Condition aggravated | |
| 117477313 | 11747731 | Dementia | |
| 117477313 | 11747731 | Drug ineffective | |
| 117477313 | 11747731 | Fatigue | |
| 117477313 | 11747731 | Hypoacusis | |
| 117477313 | 11747731 | Influenza | |
| 117477313 | 11747731 | Joint range of motion decreased | |
| 117477313 | 11747731 | Joint stiffness | |
| 117477313 | 11747731 | Pain | |
| 117477313 | 11747731 | Sleep disorder |
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 |
|---|---|---|---|---|---|---|
| 117477313 | 11747731 | 1 | 20141021 | 0 | ||
| 117477313 | 11747731 | 2 | 20130220 | 0 | ||
| 117477313 | 11747731 | 3 | 20140714 | 0 |