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
121873805 12187380 5 F 20160312 20160704 20160317 20160708 EXP CA-PFIZER INC-2016159910 PFIZER 78.00 YR F Y 0.00000 20160708 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
121873805 12187380 1 PS XELJANZ TOFACITINIB CITRATE 1 Oral 5 MG, 2X/DAY Y 203214 5 MG TABLET BID
121873805 12187380 2 SS XELJANZ TOFACITINIB CITRATE 1 Oral 5 MG, 2X/DAY Y 203214 5 MG TABLET BID
121873805 12187380 3 SS CELEBREX CELECOXIB 1 Oral UNK 20998 CAPSULE, HARD
121873805 12187380 4 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Oral UNK Y 11719

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121873805 12187380 1 Rheumatoid arthritis
121873805 12187380 3 Rheumatoid arthritis
121873805 12187380 4 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
121873805 12187380 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
121873805 12187380 Back pain
121873805 12187380 Fatigue
121873805 12187380 Gastroenteritis viral
121873805 12187380 Herpes zoster
121873805 12187380 Nephrolithiasis
121873805 12187380 Urinary tract discomfort
121873805 12187380 Vomiting

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
121873805 12187380 1 20150509 20160312 0
121873805 12187380 2 20160314 201603 0
121873805 12187380 4 20160621 0