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
126819011 12681901 1 I 20160803 20160816 20160824 20160824 EXP GB-MHRA-EYC 00143637 GB-MYLANLABS-2016M1034603 MYLAN 0.00 Y 0.00000 20160824 PH 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
126819011 12681901 1 PS OLANZAPINE. OLANZAPINE 1 UNK U U 202285
126819011 12681901 2 SS CLOMIPRAMINE CLOMIPRAMINE 1 UNK U U 0
126819011 12681901 3 SS ARIPIPRAZOLE. ARIPIPRAZOLE 1 UNK U U 0
126819011 12681901 4 SS LITHIUM CARBONATE. LITHIUM CARBONATE 1 Oral AT NIGHT Y U 0 600 MG QD
126819011 12681901 5 SS METFORMIN METFORMIN HYDROCHLORIDE 1 UNK U U 0
126819011 12681901 6 SS WARFARIN WARFARIN 1 UNK U U 0
126819011 12681901 7 C ATORVASTATIN ATORVASTATIN 1 UNK U 0
126819011 12681901 8 C LANTUS INSULIN GLARGINE 1 UNK U 0
126819011 12681901 9 C NOVORAPID INSULIN ASPART 1 UNK U 0
126819011 12681901 10 C OMEPRAZOLE. OMEPRAZOLE 1 UNK U 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126819011 12681901 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126819011 12681901 Acute kidney injury
126819011 12681901 Hypotension
126819011 12681901 International normalised ratio abnormal
126819011 12681901 Overdose
126819011 12681901 Polyuria

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
126819011 12681901 4 20160801 0