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
100122492 10012249 2 F 201312 20140318 20140314 20140331 PER 2014SP001238 STRIDES 63.00 YR F Y 0.00000 20140314 N OT 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
100122492 10012249 1 PS METHOTREXATE 1 INTRAMUSCULAR D 201529 17.5 MG
100122492 10012249 2 SS OMEPRAZOLE 1 ORAL D 0 40 MG
100122492 10012249 3 C AMLODIPINE 1 D 0
100122492 10012249 4 C CALCIUM CARBONATE 1 D 0
100122492 10012249 5 C CHOLECALCIFEROL 1 D 0
100122492 10012249 6 C VITAMIN D3 1 D 0
100122492 10012249 7 C FOLIC ACID 1 D 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100122492 10012249 1 Rheumatoid arthritis
100122492 10012249 2 Gastrooesophageal reflux disease

Outcome of event

Event ID CASEID OUTC COD
100122492 10012249 DS
100122492 10012249 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
100122492 10012249 Drug interaction
100122492 10012249 Hypomagnesaemia

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
100122492 10012249 1 20130816 20140203 0
100122492 10012249 2 20101129 201312 0