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
97303954 9730395 4 F 20130729 20160711 20131202 20160718 EXP GB-ELI_LILLY_AND_COMPANY-GB201311005900 ELI LILLY AND CO 53.00 YR M Y 0.00000 20160718 CN GB GB

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
97303954 9730395 1 PS CYMBALTA DULOXETINE HYDROCHLORIDE 1 Oral 60 MG, UNKNOWN 21427 60 MG
97303954 9730395 2 SS CLOZARIL CLOZAPINE 1 Oral UNK 0
97303954 9730395 3 SS CLOZARIL CLOZAPINE 1 Oral 225 MG, UNK 0 225 MG
97303954 9730395 4 SS CLOZARIL CLOZAPINE 1 Oral 300 MG, UNK 0 300 MG
97303954 9730395 5 SS AMINOPHYLLINE. AMINOPHYLLINE 1 Oral 300 MG, UNK 0 300 MG
97303954 9730395 6 SS PRIADEL /00033702/ LITHIUM CARBONATE 1 200 MG, UNKNOWN U U 0 200 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
97303954 9730395 1 Product used for unknown indication
97303954 9730395 2 Schizophrenia
97303954 9730395 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
97303954 9730395 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
97303954 9730395 Anaemia
97303954 9730395 Haemoglobin decreased
97303954 9730395 White blood cell count 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
97303954 9730395 2 20010701 0