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
126196661 12619666 1 I 20160601 20160721 20160803 20160803 EXP NL-LRB-221948 NL-PFIZER INC-2016367604 PFIZER 76.00 YR F Y 70.00000 KG 20160803 OT NL NL

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
126196661 12619666 1 PS PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 Oral 20 MG, QD Y 20987 20 MG TABLET QD
126196661 12619666 2 I METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Oral 5 MG, 1/WEEK U 11719 5 MG TABLET /wk
126196661 12619666 3 C FOLIUMZUUR FOLIC ACID 1 Oral 5 MG, 3/WEEK 0 5 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126196661 12619666 1 Abdominal discomfort
126196661 12619666 2 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
126196661 12619666 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126196661 12619666 Condition aggravated
126196661 12619666 Drug interaction
126196661 12619666 Rheumatoid arthritis

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
126196661 12619666 1 2011 20160601 0
126196661 12619666 2 2009 0
126196661 12619666 3 2009 0