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
126190921 12619092 1 I 20160727 20160803 20160803 PER US-ELI_LILLY_AND_COMPANY-US201607012460 ELI LILLY AND CO 0.00 F Y 0.00000 20160803 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
126190921 12619092 1 PS CYMBALTA DULOXETINE HYDROCHLORIDE 1 Unknown 20 MG, BID U 21427 20 MG CAPSULE BID
126190921 12619092 2 SS CYMBALTA DULOXETINE HYDROCHLORIDE 1 Unknown 20 MG, QD U 21427 20 MG CAPSULE QD
126190921 12619092 3 SS CYMBALTA DULOXETINE HYDROCHLORIDE 1 Unknown UNK UNK, UNKNOWN U 21427 CAPSULE
126190921 12619092 4 SS DULOXETINE HYDROCHLORIDE. DULOXETINE HYDROCHLORIDE 1 Unknown 20 MG, BID U 0 20 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126190921 12619092 1 Depression
126190921 12619092 4 Depression

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126190921 12619092 Bladder disorder
126190921 12619092 Blood oestrogen increased
126190921 12619092 Cold sweat
126190921 12619092 Diarrhoea
126190921 12619092 Drug ineffective
126190921 12619092 Feeling abnormal
126190921 12619092 Feeling hot
126190921 12619092 Hyperhidrosis
126190921 12619092 Intentional product misuse
126190921 12619092 Wrong technique in product usage process

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

no results found

Therapies reported

no results found