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
126404772 12640477 2 F 2009 20160829 20160810 20160902 EXP US-PFIZER INC-2016376457 PFIZER 65.00 YR F Y 0.00000 20160902 CN US US

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
126404772 12640477 1 PS XELJANZ TOFACITINIB CITRATE 1 5 MG, UNK U 203214 5 MG TABLET
126404772 12640477 2 SS XELJANZ TOFACITINIB CITRATE 1 UNK, 2X/DAY U 203214 TABLET BID
126404772 12640477 3 SS XELJANZ TOFACITINIB CITRATE 1 UNK U 203214 TABLET
126404772 12640477 4 SS FOLIC ACID. FOLIC ACID 1 40 MG, UNK U 5897 40 MG
126404772 12640477 5 SS FAMOTIDINE. FAMOTIDINE 1 40 MG, UNK U 0 40 MG
126404772 12640477 6 SS BUPROPION. BUPROPION 1 UNK, 2X/DAY U 0 BID
126404772 12640477 7 C HYDROCODONE/ACETAMINOPHEN ACETAMINOPHENHYDROCODONE 1 UNK, 3X/DAY (2 EVERY 8 HOUR) 0 TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126404772 12640477 1 Rheumatoid arthritis
126404772 12640477 4 Hypovitaminosis
126404772 12640477 5 Antacid therapy
126404772 12640477 6 Antidepressant therapy
126404772 12640477 7 Pain

Outcome of event

Event ID CASEID OUTC COD
126404772 12640477 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126404772 12640477 Cataract
126404772 12640477 Pain

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
126404772 12640477 2 2014 0
126404772 12640477 3 2015 0
126404772 12640477 4 2008 0
126404772 12640477 5 2007 0
126404772 12640477 6 2007 0