The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
6771430 7426837 I 6771430-8 20100529 20100614 EXP AUR-APL-2010-01427 AUROBINDO PHARMA USA 52 YR M N 20100611 OT 20100107

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
6771430 1013874154 PS FLUOXETINE 1 D D 78619
6771430 1013906984 SS CLOZARIL 1 ORAL 300MG, ORAL D D
6771430 1013907021 C FERROUS SULFATE TAB 1
6771430 1013907022 C FOLIC ACID 1
6771430 1013907023 C VITAMIN B-12 1
6771430 1013907024 C UNSPECIFIED INHALERS 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
6771430 1013906984 SCHIZOPHRENIA

Outcome of event

Event ID OUTC COD
6771430 DE
6771430 OT

Reactions reported

Event ID PT
6771430 ANAEMIA VITAMIN B12 DEFICIENCY
6771430 BEREAVEMENT
6771430 BLOOD PRESSURE INCREASED
6771430 CARDIAC DISORDER
6771430 DEPRESSED MOOD
6771430 DRUG INTERACTION
6771430 HALLUCINATION, AUDITORY
6771430 HEART RATE INCREASED
6771430 HERNIA
6771430 INCORRECT DOSE ADMINISTERED
6771430 LETHARGY
6771430 SOCIAL AVOIDANT BEHAVIOUR
6771430 STRESS
6771430 SUICIDE ATTEMPT

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

Event ID RPSR COD
6771430 FGN
6771430 HP
6771430 OTH

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6771430 1013906984 20020130