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
125411751 12541175 1 I 20160627 20160708 20160708 EXP PR 34538 US-AKORN-34538 AKORN 61.00 YR M Y 103.00000 KG 20160708 PH COUNTRY NOT SPECIFIED 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
125411751 12541175 1 PS GABAPENTIN. GABAPENTIN 1 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125411751 12541175 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125411751 12541175 Fatigue
125411751 12541175 Neck pain
125411751 12541175 Pain
125411751 12541175 Rash erythematous
125411751 12541175 Swelling
125411751 12541175 Urticaria

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

no results found

Therapies reported

no results found