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
119398893 11939889 3 F 201512 20160803 20160122 20160815 PER US-TEVA-627847USA TEVA 44.30 YR M Y 0.00000 20160815 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
119398893 11939889 1 PS COPAXONE GLATIRAMER ACETATE 1 Subcutaneous V01761 20622 40 MG INJECTION TIW
119398893 11939889 2 C CEREFOLIN CYANOCOBALAMIN CO-57LEVOMEFOLATE CALCIUMPYRIDOXINE HYDROCHLORIDERIBOFLAVIN 1 Unknown 0
119398893 11939889 3 C FLOVENT FLUTICASONE PROPIONATE 1 Unknown 0
119398893 11939889 4 C LEVOFLOXACIN. LEVOFLOXACIN 1 Unknown 0
119398893 11939889 5 C SERTRALINE SERTRALINE HYDROCHLORIDE 1 Unknown 0
119398893 11939889 6 C DULOXETINE. DULOXETINE 1 Unknown 0
119398893 11939889 7 C Nortriptyline NORTRIPTYLINE 1 0
119398893 11939889 8 C OXCARBAZEPINE. OXCARBAZEPINE 1 0
119398893 11939889 9 C PROAIR HFA ALBUTEROL SULFATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119398893 11939889 1 Multiple sclerosis
119398893 11939889 2 Product used for unknown indication
119398893 11939889 3 Product used for unknown indication
119398893 11939889 4 Product used for unknown indication
119398893 11939889 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
119398893 11939889 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119398893 11939889 Abdominal pain
119398893 11939889 Drug dose omission
119398893 11939889 Multiple sclerosis relapse
119398893 11939889 Non-cardiac chest pain
119398893 11939889 Pain in extremity

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
119398893 11939889 1 201504 0