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
5294031 6124407 F 3 5294031-X 20060628 20070323 20070405 EXP 007998 BARR LABORATORIES 1 DY M N 3 KG 20070404 OT UNITED STATES

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
5294031 1008358145 PS CLARAVIS 1 D D 76135

Indications of drugs used

no results found

Outcome of event

Event ID OUTC COD
5294031 CA
5294031 OT

Reactions reported

Event ID PT
5294031 ANOTIA
5294031 ATRIAL SEPTAL DEFECT
5294031 CEREBELLAR HYPOPLASIA
5294031 COARCTATION OF THE AORTA
5294031 CONGENITAL JOINT MALFORMATION
5294031 DANDY-WALKER SYNDROME
5294031 DRUG EXPOSURE DURING PREGNANCY
5294031 DYSKINESIA
5294031 FORCEPS DELIVERY
5294031 HEART DISEASE CONGENITAL
5294031 INTERRUPTION OF AORTIC ARCH
5294031 MITRAL VALVE HYPOPLASIA
5294031 SEPSIS NEONATAL
5294031 SINGLE FUNCTIONAL KIDNEY
5294031 TAKAYASU'S ARTERITIS
5294031 TERATOGENICITY
5294031 VENTRICULAR INTERNAL DIAMETER ABNORMAL
5294031 VENTRICULAR SEPTAL DEFECT

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

Event ID RPSR COD
5294031 CSM
5294031 HP
5294031 OTH

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
5294031 1008358145 20051025 20051110