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
121871663 12187166 3 F 20130608 20160714 20160317 20160722 EXP JP-ROCHE-1727505 ROCHE 72.72 YR M Y 0.00000 20160722 MD JP JP

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
121871663 12187166 1 PS LUCENTIS RANIBIZUMAB 1 Other 125156 .05 ML SOLUTION FOR INJECTION
121871663 12187166 2 SS LUCENTIS RANIBIZUMAB 1 Other 125156 .05 ML SOLUTION FOR INJECTION
121871663 12187166 3 SS LUCENTIS RANIBIZUMAB 1 Other 125156 .05 ML SOLUTION FOR INJECTION
121871663 12187166 4 SS LUCENTIS RANIBIZUMAB 1 Other 125156 .05 ML SOLUTION FOR INJECTION
121871663 12187166 5 C FLOMOX (CEFCAPENE PIVOXIL HYDROCHLORIDE) CEFCAPENE PIVOXIL HYDROCHLORIDE 1 Oral 0 300 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121871663 12187166 1 Age-related macular degeneration
121871663 12187166 5 Infection prophylaxis

Outcome of event

Event ID CASEID OUTC COD
121871663 12187166 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
121871663 12187166 Cerebral infarction

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
121871663 12187166 1 20110831 0
121871663 12187166 2 20130603 0
121871663 12187166 3 201307 0
121871663 12187166 4 20140127 20140127 0
121871663 12187166 5 20130603 20130608 0