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
126035081 12603508 1 I 20150409 20150414 20160728 20160728 EXP IT-MINISAL02-302492 IT-PFIZER INC-2835569 PFIZER 73.00 YR F Y 0.00000 20160728 PH 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
126035081 12603508 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Intramuscular 12.5 MG, WEEKLY Y 11719 12.5 MG SOLUTION FOR INJECTION /wk
126035081 12603508 2 SS MEDROL METHYLPREDNISOLONE 1 Oral 1 DF, 1X/DAY 11153 1 DF TABLET QD
126035081 12603508 3 C FOLINA /00024201/ FOLIC ACID 1 UNK 0
126035081 12603508 4 C METOCAL 2 UNK 0
126035081 12603508 5 C OLPRESS OLMESARTAN MEDOXOMIL 1 UNK 0
126035081 12603508 6 C ZEFFIX LAMIVUDINE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126035081 12603508 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
126035081 12603508 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126035081 12603508 Immunosuppression
126035081 12603508 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
126035081 12603508 1 20070101 20150409 0
126035081 12603508 2 20070101 0