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
127989101 12798910 1 I 20160927 20160930 20160930 PER US-ELI_LILLY_AND_COMPANY-US201609010530 ELI LILLY AND CO 0.00 F Y 0.00000 20160930 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
127989101 12798910 1 PS DULOXETINE HYDROCHLORIDE. DULOXETINE HYDROCHLORIDE 1 Unknown 30 MG, QD D 21427 30 MG QD
127989101 12798910 2 SS DULOXETINE HYDROCHLORIDE. DULOXETINE HYDROCHLORIDE 1 20 MG, QD D 21427 20 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127989101 12798910 1 Pain
127989101 12798910 2 Fibromyalgia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127989101 12798910 Anxiety
127989101 12798910 Diarrhoea
127989101 12798910 Dizziness
127989101 12798910 Fatigue
127989101 12798910 Headache
127989101 12798910 Hyperhidrosis
127989101 12798910 Hypoaesthesia
127989101 12798910 Insomnia
127989101 12798910 Irritability
127989101 12798910 Nausea
127989101 12798910 Paraesthesia
127989101 12798910 Rash
127989101 12798910 Vomiting
127989101 12798910 Withdrawal syndrome

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
127989101 12798910 1 2015 0
127989101 12798910 2 20160917 0