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
127810841 12781084 1 I 20160722 20160913 20160926 20160926 EXP GB-ELI_LILLY_AND_COMPANY-GB201609004378 ELI LILLY AND CO 42.00 YR M Y 0.00000 20160923 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
127810841 12781084 1 PS OLANZAPINE. OLANZAPINE 1 Oral 22.5 MG, QD Y U 20592 22.5 MG QD
127810841 12781084 2 SS OLANZAPINE. OLANZAPINE 1 Oral 20 MG, QD Y U 20592 20 MG QD
127810841 12781084 3 SS CLOZARIL CLOZAPINE 1 Oral 300 MG, QD 5400 MG Y U 0 300 MG QD
127810841 12781084 4 SS CLOZARIL CLOZAPINE 1 Oral 50 MG, EACH MORNING 5400 MG Y U 0 50 MG QD
127810841 12781084 5 SS CLOZARIL CLOZAPINE 1 Oral UNK 5400 MG Y U 0
127810841 12781084 6 C CHOLECALCIFEROL CHOLECALCIFEROL 1 Unknown UNK UNK, UNKNOWN U U 0
127810841 12781084 7 C EPILIM VALPROATE SODIUM 1 Oral 900 MG, BID 0 900 MG BID
127810841 12781084 8 C FOLIC ACID. FOLIC ACID 1 Oral 5 MG, QD 0 5 MG QD
127810841 12781084 9 C GLICLAZIDE GLICLAZIDE 1 Oral 80 MG, QD 0 80 MG QD
127810841 12781084 10 C LAMOTRIGINE. LAMOTRIGINE 1 Oral 200 MG, QD 0 200 MG QD
127810841 12781084 11 C LEVETIRACETAM. LEVETIRACETAM 1 Oral 500 MG, BID 0 500 MG BID
127810841 12781084 12 C METFORMIN METFORMIN HYDROCHLORIDE 1 Oral 500 MG, TID 0 500 MG TID
127810841 12781084 13 C SERTRALINE SERTRALINE HYDROCHLORIDE 1 Oral 150 MG, QD 0 150 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127810841 12781084 1 Psychotic disorder
127810841 12781084 3 Schizophrenia
127810841 12781084 4 Psychotic disorder
127810841 12781084 6 Product used for unknown indication
127810841 12781084 7 Epilepsy
127810841 12781084 8 Product used for unknown indication
127810841 12781084 9 Type 2 diabetes mellitus
127810841 12781084 10 Epilepsy
127810841 12781084 11 Epilepsy
127810841 12781084 12 Type 2 diabetes mellitus
127810841 12781084 13 Depression

Outcome of event

Event ID CASEID OUTC COD
127810841 12781084 HO
127810841 12781084 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127810841 12781084 Aphasia
127810841 12781084 Blood calcium decreased
127810841 12781084 Blood cholesterol decreased
127810841 12781084 Confusional state
127810841 12781084 Dyspnoea
127810841 12781084 Dysstasia
127810841 12781084 Fall
127810841 12781084 Haematocrit decreased
127810841 12781084 Haemoglobin decreased
127810841 12781084 Lymphocyte count increased
127810841 12781084 Malaise
127810841 12781084 Mean cell volume increased
127810841 12781084 Neutrophil count increased
127810841 12781084 Pharyngitis
127810841 12781084 Prescribed overdose
127810841 12781084 Pyrexia
127810841 12781084 Red blood cell count decreased
127810841 12781084 Respiratory rate increased
127810841 12781084 Seizure
127810841 12781084 Somnolence
127810841 12781084 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
127810841 12781084 1 2008 0
127810841 12781084 2 20160723 0
127810841 12781084 3 20160704 0
127810841 12781084 5 20160723 0