The Safety Rates Drug Report

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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
123986432 12398643 2 F 20160816 20160524 20160823 EXP CA-PFIZER INC-2015300227 PFIZER 0.00 A F Y 0.00000 20160823 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
123986432 12398643 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Oral 15 MG, WEEKLY 11719 15 MG TABLET /wk
123986432 12398643 2 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Oral 6 DF, WEEKLY 11719 6 DF TABLET /wk
123986432 12398643 3 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Oral 15 MG, WEEKLY 11719 15 MG TABLET /wk
123986432 12398643 4 SS SULFASALAZINE. SULFASALAZINE 1 Oral UNK, DAILY Y 7073
123986432 12398643 5 SS SULFASALAZINE. SULFASALAZINE 1 Oral 500 MG, 2X/DAY Y 7073 500 MG BID
123986432 12398643 6 SS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Oral 1 DF, 1X/DAY Y 0 1 DF TABLET QD
123986432 12398643 7 SS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Oral 200 MG, 2X/DAY Y 0 200 MG TABLET BID
123986432 12398643 8 C PREDNISONE. PREDNISONE 1 Oral 1 DF, 1X/DAY 0 1 DF TABLET QD
123986432 12398643 9 C LEFLUNOMIDE. LEFLUNOMIDE 1 Oral 1 DF, 1X/DAY 0 1 DF TABLET QD
123986432 12398643 10 C HYDROTHIAZIDE 2 Oral 1 DF, 1X/DAY 0 1 DF TABLET QD
123986432 12398643 11 C FOLIC ACID. FOLIC ACID 1 Oral 1 DF ONCE DAILY EXCEPT ON DAYS WHEN PATIENT TAKES METHOTREXATE 0 1 DF TABLET
123986432 12398643 12 C GLUCOSAMINE GLUCOSAMINE 1 Oral UNK, 1X/DAY 0 QD
123986432 12398643 13 C MULTIVITAMINS VITAMINS 1 Oral UNK, 1X/DAY 0 QD
123986432 12398643 14 C VITAMIN C ASCORBIC ACID 1 Oral UNK, 1X/DAY 0 QD
123986432 12398643 15 C VITAMIN D CHOLECALCIFEROL 1 Oral UNK, 1X/DAY 0 QD
123986432 12398643 16 C TYLENOL ARTHRITIS PAIN ACETAMINOPHEN 1 UNK, AS NEEDED 0
123986432 12398643 17 C TOVIAZ FESOTERODINE FUMARATE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123986432 12398643 1 Rheumatoid arthritis
123986432 12398643 4 Rheumatoid arthritis
123986432 12398643 6 Rheumatoid arthritis
123986432 12398643 8 Rheumatoid arthritis
123986432 12398643 9 Rheumatoid arthritis
123986432 12398643 16 Pain
123986432 12398643 17 Pollakiuria

Outcome of event

Event ID CASEID OUTC COD
123986432 12398643 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123986432 12398643 Bladder disorder
123986432 12398643 Cystitis
123986432 12398643 Malaise
123986432 12398643 Peripheral swelling
123986432 12398643 Pollakiuria
123986432 12398643 Retinal toxicity

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
123986432 12398643 4 201411 0
123986432 12398643 5 201508 0
123986432 12398643 6 201310 0
123986432 12398643 7 201408 0