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
126148251 12614825 1 I 20160608 20160727 20160802 20160802 EXP CH-SM-2016-06025 CH-PFIZER INC-2016364067 PFIZER 30.00 YR F Y 78.00000 KG 20160802 MD CH CH

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
126148251 12614825 1 PS SOLU-MEDROL METHYLPREDNISOLONE SODIUM SUCCINATE 1 Intravenous drip 1 G, 1X/DAY 3 G Y 11856 1 G POWDER FOR SOLUTION FOR INJECTION QD
126148251 12614825 2 SS SOLU-MEDROL METHYLPREDNISOLONE SODIUM SUCCINATE 1 Intravenous drip 0.5 G, 1X/DAY 3 G Y 11856 .5 G POWDER FOR SOLUTION FOR INJECTION QD
126148251 12614825 3 SS COPAXONE GLATIRAMER ACETATE 1 Subcutaneous 20 MG, 1X/DAY 0 20 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126148251 12614825 1 Relapsing-remitting multiple sclerosis
126148251 12614825 3 Relapsing-remitting multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
126148251 12614825 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126148251 12614825 Abdominal pain
126148251 12614825 Gastritis
126148251 12614825 Liver injury
126148251 12614825 Nausea

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
126148251 12614825 1 20160606 20160608 0
126148251 12614825 2 20160609 20160609 0
126148251 12614825 3 20160204 0