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
126583642 12658364 2 F 201506 20160907 20160817 20160913 EXP DE-ROCHE-1814797 ROCHE 0.00 A M Y 0.00000 20160913 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
126583642 12658364 1 PS LUCENTIS RANIBIZUMAB 1 Unknown UNK 125156 SOLUTION FOR INJECTION
126583642 12658364 2 SS LUCENTIS RANIBIZUMAB 1 Unknown UNK 125156 SOLUTION FOR INJECTION
126583642 12658364 3 C FALITHROM PHENPROCOUMON 1 Unknown U 0
126583642 12658364 4 C Torasemide TORSEMIDE 1 Unknown U 0
126583642 12658364 5 C INSULIN INSULIN NOS 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126583642 12658364 1 Product used for unknown indication
126583642 12658364 3 Product used for unknown indication
126583642 12658364 4 Product used for unknown indication
126583642 12658364 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126583642 12658364 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126583642 12658364 Myocardial 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
126583642 12658364 1 201401 201401 0
126583642 12658364 2 201405 0