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
127809881 12780988 1 I 20160916 20160926 20160926 EXP GB-MHRA-EYC 00145104 GB-MYLANLABS-2016M1040176 MYLAN 0.00 Y 0.00000 20160926 MD 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
127809881 12780988 1 PS QUETIAPINE. QUETIAPINE 1 UNK(PRESCRIBED DOSE: 300MG AT NIGHT) D U 90323
127809881 12780988 2 SS PREGABALIN. PREGABALIN 1 UNK(PRESCRIBED DOSE: 450MG DAILY) D U 0
127809881 12780988 3 C SERTRALINE SERTRALINE HYDROCHLORIDE 1 200 MG, QD U 0 200 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127809881 12780988 2 Depression

Outcome of event

Event ID CASEID OUTC COD
127809881 12780988 DE
127809881 12780988 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127809881 12780988 Brain hypoxia
127809881 12780988 Depressed level of consciousness
127809881 12780988 Ketoacidosis
127809881 12780988 Overdose
127809881 12780988 Somnolence
127809881 12780988 Toxicity to various agents

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
127809881 12780988 2 201502 0