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
115456432 11545643 2 F 20150409 20160725 20150924 20160728 EXP IT-PFIZER INC-2015130820 PFIZER 73.00 YR F Y 0.00000 20160728 OT IT IT

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
115456432 11545643 1 PS METHOTREXATE (METHOTREXATE SODIUM) METHOTREXATE SODIUM 1 Intramuscular 12.5 MG, WEEKLY 5412 MG Y 11719 12.5 MG /wk
115456432 11545643 2 SS MEDROL METHYLPREDNISOLONE 1 Oral 1 DF, DAILY 11153 1 DF TABLET
115456432 11545643 3 C ZEFFIX LAMIVUDINE 1 0
115456432 11545643 4 C FOLINA /00024201/ FOLIC ACID 1 0
115456432 11545643 5 C OLPRESS OLMESARTAN MEDOXOMIL 1 0
115456432 11545643 6 C METOCAL 2 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
115456432 11545643 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
115456432 11545643 OT
115456432 11545643 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
115456432 11545643 Immunosuppression
115456432 11545643 Urinary tract infection

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
115456432 11545643 1 20070101 20150409 0
115456432 11545643 2 20070101 0