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
6699221 7368031 I 6699221-7 20100130 20100416 20100427 EXP GB-TEVA-231816ISR TEVA 88 YR M Y 65 KG 20100427 OT UNITED KINGDOM

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
6699221 1013579877 PS BRIMONIDINE 2 OPHTHALMIC 76372
6699221 1013579878 SS DORZOLAMIDE 1 OPHTHALMIC
6699221 1013579879 SS ACETYLSALICYLIC ACID 2 ORAL
6699221 1013579880 SS FOLIC ACID 1 ORAL
6699221 1013579881 SS GANFORT (BIMATOPROST, TIMOLOL) 2 OPHTHALMIC
6699221 1013579882 SS MOVICOL 2 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
6699221 1013579877 GLAUCOMA
6699221 1013579878 GLAUCOMA
6699221 1013579879 ATRIAL FIBRILLATION
6699221 1013579880 ANAEMIA
6699221 1013579881 GLAUCOMA
6699221 1013579882 CONSTIPATION

Outcome of event

Event ID OUTC COD
6699221 OT

Reactions reported

Event ID PT
6699221 NEPHROPATHY TOXIC

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
6699221 1013579877 20051019
6699221 1013579878 20041101
6699221 1013579879 20011116
6699221 1013579880 20040604
6699221 1013579881 20080919
6699221 1013579882 20051013