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
125557382 12555738 2 F 2016 20160711 20160714 20160715 PER US-PFIZER INC-2016340428 PFIZER 76.00 YR F Y 75.11000 KG 20160715 CN 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
125557382 12555738 1 PS LYRICA PREGABALIN 1 200 MG AT NIGHT AND 150 MG IN THE MORNING Y 21446
125557382 12555738 2 SS LYRICA PREGABALIN 1 150 MG AT NIGHT AND 150 MG IN THE MORNING Y 21446
125557382 12555738 3 SS CYMBALTA DULOXETINE HYDROCHLORIDE 1 30 MG, ONCE A DAY Y 0 30 MG QD
125557382 12555738 4 SS CYMBALTA DULOXETINE HYDROCHLORIDE 1 Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125557382 12555738 1 Fibromyalgia
125557382 12555738 3 Pain
125557382 12555738 4 Neuralgia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125557382 12555738 Discomfort
125557382 12555738 Drug ineffective
125557382 12555738 Intentional product misuse
125557382 12555738 Malaise
125557382 12555738 Nausea
125557382 12555738 Oral mucosal blistering
125557382 12555738 Product label issue
125557382 12555738 Swelling
125557382 12555738 Weight increased

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
125557382 12555738 1 2016 0
125557382 12555738 3 2016 2016 0