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
5578152 6472603 F 5578152-X 20010101 20071219 20071231 EXP BR-PFIZER INC-2007096537 PFIZER INC F Y 20071231 BRAZIL

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
5578152 1009350731 PS XALATAN 1 OPHTHALMIC 020597
5578152 1009350732 SS XALATAN 1 OPHTHALMIC DAILY DOSE:1DROP 020597
5578152 1009350733 SS XALATAN 1 020597
5578152 1009350734 SS LUMIGAN 1
5578152 1009350735 C SENNA 2
5578152 1009350736 C DUSPATALIN ^SOLVAY^ 2
5578152 1009350737 C BETAHISTINE 2 DAILY DOSE:16MG
5578152 1009350738 C SIMVASTATIN 1 DAILY DOSE:20MG
5578152 1009350739 C ANTIDEPRESSANTS 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
5578152 1009350731 GLAUCOMA
5578152 1009350735 CONSTIPATION
5578152 1009350736 GASTRITIS
5578152 1009350737 LABYRINTHITIS
5578152 1009350738 BLOOD CHOLESTEROL INCREASED
5578152 1009350739 DEPRESSION

Outcome of event

Event ID OUTC COD
5578152 HO
5578152 OT

Reactions reported

Event ID PT
5578152 EYE INFECTION
5578152 GLAUCOMA
5578152 LABYRINTHITIS

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
5578152 1009350732 20020101 20060101