The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
6138281 6869877 F 6138281-9 20081128 20090316 20090331 EXP US-GENENTECH-274262 GNEFDAAERSPRD 79 M Y 20090331 MD 20081128 SWITZERLAND

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
6138281 1011356988 PS RANIBIZUMAB 2 UNKNOWN UNK NOT REPORTED
6138281 1011356989 C MEXILETINE HYDROCHLORIDE 1
6138281 1011356990 C LISINOPRIL 1
6138281 1011356991 C SIMVASTATIN 1
6138281 1011356992 C WARFARIN SODIUM 1
6138281 1011356993 C TAMSULOSIN HYDROCHLORIDE 2
6138281 1011356994 C FUROSEMIDE 1
6138281 1011356995 C POTASSIUM CHLORIDE 1
6138281 1011356996 C GOSERELIN 2
6138281 1011356997 C NAPROXEN 1
6138281 1011356998 C LUTEIN 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
6138281 1011356988 MACULAR DEGENERATION
6138281 1011356989 DRUG USE FOR UNKNOWN INDICATION
6138281 1011356990 DRUG USE FOR UNKNOWN INDICATION
6138281 1011356991 DRUG USE FOR UNKNOWN INDICATION
6138281 1011356992 DRUG USE FOR UNKNOWN INDICATION
6138281 1011356993 DRUG USE FOR UNKNOWN INDICATION
6138281 1011356994 DRUG USE FOR UNKNOWN INDICATION
6138281 1011356995 DRUG USE FOR UNKNOWN INDICATION
6138281 1011356996 DRUG USE FOR UNKNOWN INDICATION
6138281 1011356997 DRUG USE FOR UNKNOWN INDICATION
6138281 1011356998 DRUG USE FOR UNKNOWN INDICATION

Outcome of event

Event ID OUTC COD
6138281 DE

Reactions reported

Event ID PT
6138281 ARTERIOSCLEROSIS

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6138281 1011356988 20080306