The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
127126693 12712669 3 F 20160720 20160921 20160902 20160926 EXP FR-ALLERGAN-1667582US ALLERGAN 69.00 YR M Y 72.00000 KG 20160926 MD FR FR

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
127126693 12712669 1 PS LUMIGAN BIMATOPROST 1 Ophthalmic 1 GTT, QD 16 Gtt U U 22184 1 GTT EYE DROPS, SOLUTION QD
127126693 12712669 2 SS COMBIGAN BRIMONIDINE TARTRATETIMOLOL MALEATE 1 UNK 0 EYE DROPS, SOLUTION
127126693 12712669 3 C Zanidip LERCANIDIPINE HYDROCHLORIDE 1 Oral 1 DF, QD U 0 1 DF QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127126693 12712669 1 Glaucoma
127126693 12712669 2 Glaucoma
127126693 12712669 3 Hypertension

Outcome of event

Event ID CASEID OUTC COD
127126693 12712669 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127126693 12712669 Choroidal detachment
127126693 12712669 Hypotony of eye
127126693 12712669 Macular oedema

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
127126693 12712669 1 20160705 20160801 0
127126693 12712669 2 201506 0
127126693 12712669 3 2010 0