The Safety Rates Drug Report

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Drug     Injury     Quarter    

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
124902163 12490216 3 F 20160303 20160831 20160622 20160906 EXP CA-PFIZER INC-2016145236 PFIZER 59.00 YR F Y 0.00000 20160906 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
124902163 12490216 1 PS XELJANZ TOFACITINIB CITRATE 1 Oral 5 MG, 2X/DAY 203214 5 MG TABLET BID
124902163 12490216 2 SS CELEBREX CELECOXIB 1 Oral UNK 20998 CAPSULE, HARD
124902163 12490216 3 SS PREGABALIN. PREGABALIN 1 Oral UNK 21446
124902163 12490216 4 SS PREDNISONE. PREDNISONE 1 Oral 5 MG, DAILY 0 5 MG
124902163 12490216 5 C ARAVA LEFLUNOMIDE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124902163 12490216 1 Rheumatoid arthritis
124902163 12490216 2 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
124902163 12490216 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124902163 12490216 Abdominal pain
124902163 12490216 Faeces soft
124902163 12490216 Fatigue
124902163 12490216 Frequent bowel movements
124902163 12490216 Grip strength decreased
124902163 12490216 Musculoskeletal stiffness
124902163 12490216 Nasopharyngitis
124902163 12490216 Oedema peripheral
124902163 12490216 Onychoclasis
124902163 12490216 Retinopathy
124902163 12490216 Synovial cyst
124902163 12490216 Vision blurred
124902163 12490216 Vitreous adhesions

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
124902163 12490216 1 20160402 0
124902163 12490216 4 201601 0