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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126294631 | 12629463 | 1 | I | 20160728 | 20160808 | 20160808 | EXP | CA-SA-2016SA138869 | AVENTIS | 50.00 | YR | A | F | Y | 109.00000 | KG | 20160808 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126294631 | 12629463 | 1 | SS | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | Unknown | U | UNKNOWN | 0 | TABLET | ||||||||
126294631 | 12629463 | 2 | PS | LEFLUNOMIDE. | LEFLUNOMIDE | 1 | Unknown | U | UNKNOWN | 20905 | TABLET | ||||||||
126294631 | 12629463 | 3 | SS | ACTEMRA | TOCILIZUMAB | 1 | Intravenous (not otherwise specified) | FREQUENCY- 1 EVERY 4 WEEKS | U | UNKNOWN | 0 | 480 | MG | ||||||
126294631 | 12629463 | 4 | SS | ACTEMRA | TOCILIZUMAB | 1 | Intravenous (not otherwise specified) | FREQUENCY- 1 EVERY 4 WEEKS | U | UNKNOWN | 0 | 800 | MG | ||||||
126294631 | 12629463 | 5 | SS | RITUXAN | RITUXIMAB | 1 | Intravenous (not otherwise specified) | FORM- SOLUTION INTRAVENOUS | U | UNKNOWN | 0 | 1000 | MG | ||||||
126294631 | 12629463 | 6 | C | ACETAMINOPHEN. | ACETAMINOPHEN | 1 | 0 | ||||||||||||
126294631 | 12629463 | 7 | C | ADVIL | IBUPROFEN | 1 | 0 | ||||||||||||
126294631 | 12629463 | 8 | C | BENADRYL | DIPHENHYDRAMINE HYDROCHLORIDE | 1 | Oral | 0 | 50 | MG | |||||||||
126294631 | 12629463 | 9 | C | ENALAPRIL MALEATE. | ENALAPRIL MALEATE | 1 | 0 | ||||||||||||
126294631 | 12629463 | 10 | C | FLUOXETINE | FLUOXETINE HYDROCHLORIDE | 1 | 0 | ||||||||||||
126294631 | 12629463 | 11 | C | GLICLAZIDE | GLICLAZIDE | 1 | 0 | TABLET | |||||||||||
126294631 | 12629463 | 12 | C | LANTUS | INSULIN GLARGINE | 1 | FORM: SOLUTION SUBCUTANEOUS | 0 | |||||||||||
126294631 | 12629463 | 13 | C | PANTOPRAZOLE | PANTOPRAZOLE SODIUM | 1 | 0 | ||||||||||||
126294631 | 12629463 | 14 | C | PREDNISONE. | PREDNISONE | 1 | 0 | ||||||||||||
126294631 | 12629463 | 15 | C | PROVERA | MEDROXYPROGESTERONE ACETATE | 1 | 0 | ||||||||||||
126294631 | 12629463 | 16 | C | TYLENOL | ACETAMINOPHEN | 1 | Oral | 0 | 1000 | MG |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126294631 | 12629463 | 3 | Rheumatoid arthritis |
126294631 | 12629463 | 4 | Rheumatoid arthritis |
126294631 | 12629463 | 5 | Rheumatoid arthritis |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126294631 | 12629463 | OT |
126294631 | 12629463 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126294631 | 12629463 | Animal scratch | |
126294631 | 12629463 | Arthralgia | |
126294631 | 12629463 | Blood pressure diastolic decreased | |
126294631 | 12629463 | Cartilage injury | |
126294631 | 12629463 | Diarrhoea | |
126294631 | 12629463 | Drug ineffective | |
126294631 | 12629463 | Fall | |
126294631 | 12629463 | Fatigue | |
126294631 | 12629463 | Hip fracture | |
126294631 | 12629463 | Hypotension | |
126294631 | 12629463 | Impaired healing | |
126294631 | 12629463 | Insomnia | |
126294631 | 12629463 | Joint instability | |
126294631 | 12629463 | Joint swelling | |
126294631 | 12629463 | Myalgia | |
126294631 | 12629463 | Pain | |
126294631 | 12629463 | Sciatica | |
126294631 | 12629463 | Sleep disorder | |
126294631 | 12629463 | Tooth repair | |
126294631 | 12629463 | Weight decreased |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |