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
5794782 6231198 F 5794782-4 20051008 20080624 20080630 EXP A0626407A GLAXOSMITHKLINE M Y 3.6 KG 20080630 CN 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
5794782 1010109974 PS PAXIL CR 1 25MG PER DAY 20936
5794782 1010109975 C ZOLOFT 1 50MG UNKNOWN
5794782 1010109976 C TYLENOL 1
5794782 1010109977 C VALTREX 1
5794782 1010109978 C VITAMIN TAB 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
5794782 1010109974 DEPRESSION

Outcome of event

Event ID OUTC COD
5794782 CA
5794782 HO

Reactions reported

Event ID PT
5794782 ATRIAL SEPTAL DEFECT
5794782 BLOOD PRESSURE DECREASED
5794782 CARDIAC MURMUR
5794782 CONGENITAL AORTIC ANOMALY
5794782 CONGENITAL AORTIC VALVE INCOMPETENCE
5794782 CONGENITAL FOOT MALFORMATION
5794782 DRUG EXPOSURE DURING PREGNANCY
5794782 FINGER DEFORMITY
5794782 FOETAL GROWTH RETARDATION
5794782 HEART DISEASE CONGENITAL
5794782 HEART VALVE INCOMPETENCE
5794782 HYPERBILIRUBINAEMIA
5794782 JAUNDICE NEONATAL
5794782 LIMB MALFORMATION
5794782 MACROSOMIA
5794782 MARFAN'S SYNDROME
5794782 OTITIS MEDIA
5794782 PATENT DUCTUS ARTERIOSUS
5794782 PERICARDIAL EFFUSION

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
5794782 1010109974 20040706 20050301
5794782 1010109975 20050301