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
126333971 12633397 1 I 20160629 20160629 20160809 20160809 PER US-TEVA-675480USA TEVA 39.25 YR F Y 0.00000 20160809 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
126333971 12633397 1 PS COPAXONE GLATIRAMER ACETATE 1 Subcutaneous V02031 20622 TIW
126333971 12633397 2 C PROAIR HFA ALBUTEROL SULFATE 1 0
126333971 12633397 3 C HYDROCODONE BITARTRATE AND ACETAMINOPHEN ACETAMINOPHENHYDROCODONE BITARTRATE 1 0
126333971 12633397 4 C BUPROPION 150MG SR 2 0
126333971 12633397 5 C BUPROPION 250MG ER 2 0
126333971 12633397 6 C BUPROPION 300MG XL 2 0
126333971 12633397 7 C MODAFINIL. MODAFINIL 1 0
126333971 12633397 8 C LEVOCETIRIZIN LEVOCETIRIZINE DIHYDROCHLORIDE 1 0
126333971 12633397 9 C TOPIRAMATE. TOPIRAMATE 1 0
126333971 12633397 10 C ESCITALOPRAM ESCITALOPRAM OXALATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126333971 12633397 1 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126333971 12633397 Drug dose omission
126333971 12633397 Fatigue

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
126333971 12633397 1 20160108 0