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
125089332 12508933 2 F 20160526 20160905 20160629 20160919 EXP FR-SA-2016SA116383 AVENTIS 34.00 YR A F Y 0.00000 20160919 MD FR FR

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
125089332 12508933 1 PS AUBAGIO TERIFLUNOMIDE 1 Oral Y UNK 202992 1 DF TABLET QD
125089332 12508933 2 SS SOLU-MEDROL METHYLPREDNISOLONE SODIUM SUCCINATE 1 Unknown BOLUS U UNK 0 3 G
125089332 12508933 3 SS PARACETAMOL ACETAMINOPHEN 1 Oral DOSE : 1000, SIX TIMES A DAY U UNK 0 Q4H
125089332 12508933 4 SS PARACETAMOL ACETAMINOPHEN 1 Oral DOSE : 1000, SIX TIMES A DAY U UNK 0 Q4H

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125089332 12508933 1 Multiple sclerosis
125089332 12508933 2 Pain
125089332 12508933 3 Abdominal pain
125089332 12508933 4 Pain

Outcome of event

Event ID CASEID OUTC COD
125089332 12508933 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125089332 12508933 Abdominal pain
125089332 12508933 Asthenia
125089332 12508933 Cell death
125089332 12508933 Hepatitis acute
125089332 12508933 Hepatocellular injury
125089332 12508933 Vertigo

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
125089332 12508933 1 20160112 20160526 0
125089332 12508933 2 20160425 20160427 0
125089332 12508933 3 20151201 20160526 0
125089332 12508933 4 20151201 20160526 0