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
124820242 12482024 2 F 2016 20160726 20160620 20160805 EXP US-TEVA-668721USA TEVA 0.00 F Y 0.00000 20160805 PH US US

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
124820242 12482024 1 PS COPAXONE GLATIRAMER ACETATE 1 Subcutaneous V02001 20622 40 MG INJECTION TIW
124820242 12482024 2 C TEMAZEPAM. TEMAZEPAM 1 0
124820242 12482024 3 C AMITRIPTYLINE AMITRIPTYLINE 1 0
124820242 12482024 4 C VITAMIN D CHOLECALCIFEROL 1 0
124820242 12482024 5 C CEPHALEXIN. CEPHALEXIN 1 0
124820242 12482024 6 C AMANTADINE AMANTADINE 1 0
124820242 12482024 7 C PENTASA MESALAMINE 1 0
124820242 12482024 8 C VESICARE SOLIFENACIN SUCCINATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124820242 12482024 1 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
124820242 12482024 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124820242 12482024 Dyspnoea
124820242 12482024 Erythema
124820242 12482024 Shock

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

no results found

Therapies reported

no results found