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
127095781 12709578 1 I 201608 0 20160901 20160901 DIR 59.00 YR F N 0.00000 20160830 Y PH 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
127095781 12709578 1 PS REBIF INTERFERON BETA-1A 1 Subcutaneous D D A0016347 20180131 0 44 UG QW
127095781 12709578 3 C TYLENOL ACETAMINOPHEN 1 0
127095781 12709578 4 C KEFLEX CEPHALEXIN 1 0
127095781 12709578 6 C METHYLPRED METHYLPREDNISOLONE 1 0
127095781 12709578 8 C ALEVE NAPROXEN SODIUM 1 0
127095781 12709578 10 C VENLAFAXINE VENLAFAXINE HYDROCHLORIDE 1 0
127095781 12709578 12 C BONIVA IBANDRONATE SODIUM 1 0
127095781 12709578 14 C BACLOFEN. BACLOFEN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127095781 12709578 1 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127095781 12709578 Depression

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

Event ID CASEID RPSR COD
127095781 12709578 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
127095781 12709578 1 20080507 0