The Safety Rates Drug Report

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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
119931555 11993155 5 F 20150306 20160729 20160203 20160810 EXP DE-ROCHE-1705074 ROCHE 74.00 YR F Y 85.00000 KG 20160810 MD DE DE

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
119931555 11993155 1 PS Ranibizumab RANIBIZUMAB 1 Other 0.5 MG (0.05 ML), PRN U UNKNOWN 125156 .5 MG SOLUTION FOR INJECTION
119931555 11993155 2 SS Ranibizumab RANIBIZUMAB 1 Other LAST DOSE PRIOR TO SAE U UNKNOWN 125156 .5 MG SOLUTION FOR INJECTION
119931555 11993155 3 C CEFUROXIME. CEFUROXIME 1 Intraocular 1 MG, UNK U 0 1 MG
119931555 11993155 4 C CEFUROXIME. CEFUROXIME 1 Intraocular UNK U 0
119931555 11993155 5 C DEXAHEXAL 2 Intraocular 1 MG, UNK U 0 1 MG
119931555 11993155 6 C DEXAHEXAL 2 Intraocular UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119931555 11993155 1 Neovascular age-related macular degeneration
119931555 11993155 2 Age-related macular degeneration
119931555 11993155 3 Prophylaxis
119931555 11993155 5 Prophylaxis

Outcome of event

Event ID CASEID OUTC COD
119931555 11993155 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119931555 11993155 Cataract
119931555 11993155 Glaucoma

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
119931555 11993155 1 20140613 0
119931555 11993155 2 20150106 20150106 0
119931555 11993155 3 20130202 20130202 0
119931555 11993155 4 20160224 0
119931555 11993155 5 20160202 20160202 0
119931555 11993155 6 20160224 0