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
124195272 12419527 2 F 20160407 20160824 20160531 20160829 EXP GB-MHRA-EYC 00139826 GB-PFIZER INC-2016272039 PFIZER 37.00 YR F Y 65.00000 KG 20160829 MD GB GB

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
124195272 12419527 1 PS SULFASALAZINE. SULFASALAZINE 1 Oral 500 MG, 2X/DAY (INCREASING WEEKLY BY 500MG AFTER STARTING AT 500 MG TWICE A DAY) 22000 MG Y 7073 500 MG BID
124195272 12419527 2 C METHOTREXATE. METHOTREXATE 1 0
124195272 12419527 3 C VENLAFAXINE VENLAFAXINE HYDROCHLORIDE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124195272 12419527 1 Psoriatic arthropathy

Outcome of event

Event ID CASEID OUTC COD
124195272 12419527 DS
124195272 12419527 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124195272 12419527 Amnesia
124195272 12419527 Confusional state
124195272 12419527 Encephalitis
124195272 12419527 Headache
124195272 12419527 Seizure

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
124195272 12419527 1 20160316 20160407 0
124195272 12419527 2 201512 0