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
126204891 12620489 1 I 2016 20160725 20160804 20160804 EXP AU-ROCHE-1807442 ROCHE 0.00 F Y 0.00000 20160804 CN AU AU

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
126204891 12620489 1 PS LUCENTIS RANIBIZUMAB 1 Other UNK 125156 SOLUTION FOR INJECTION
126204891 12620489 2 SS XALATAN LATANOPROST 1 Unknown 1 DROP AT NIGHT N 04/207/M70341804145 0
126204891 12620489 3 SS ZINNAT CEFUROXIME AXETIL 1 Unknown 250 MG, UNK N 0 250 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126204891 12620489 1 Product used for unknown indication
126204891 12620489 2 Intraocular pressure decreased
126204891 12620489 3 Wheezing

Outcome of event

Event ID CASEID OUTC COD
126204891 12620489 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126204891 12620489 Blepharitis
126204891 12620489 Device defective
126204891 12620489 Eye irritation
126204891 12620489 Glaucoma
126204891 12620489 Inflammation
126204891 12620489 Joint range of motion decreased
126204891 12620489 Vision blurred

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
126204891 12620489 1 20100902 0
126204891 12620489 2 201007 20150423 0
126204891 12620489 3 20160624 20160714 0