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
125732941 12573294 1 I 20160706 20160720 20160720 EXP CA-PFIZER INC-2016346979 PFIZER 53.00 YR M Y 0.00000 20160720 CN CA CA

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
125732941 12573294 1 PS ALTACE RAMIPRIL 1 2.5 MG, DAILY U 19901 2.5 MG CAPSULE
125732941 12573294 2 SS MESALAMINE. MESALAMINE 1 2.4 G, DAILY U 0 2.4 G
125732941 12573294 3 SS VEDOLIZUMAB VEDOLIZUMAB 1 Intravenous (not otherwise specified) 300 MG, UNK U 0 300 MG
125732941 12573294 4 C AMLODIPINE AMLODIPINE BESYLATE 1 5 MG, 1X/DAY 0 5 MG TABLET QD
125732941 12573294 5 C PANTOLOC PANTOPRAZOLE SODIUM 1 40 MG, 1X/DAY 0 40 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125732941 12573294 3 Colitis ulcerative

Outcome of event

Event ID CASEID OUTC COD
125732941 12573294 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125732941 12573294 Blood creatinine increased
125732941 12573294 Kidney fibrosis
125732941 12573294 Nephritis

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found