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
7602871 8038745 I 7602871-4 20110406 20110620 20110630 EXP OSCN-NO-1106S-0155 GE HEALTHCARE 67 YR M N 20110629 OT NORWAY

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
7602871 1017027835 C PRAMIPEXOLE DIHYDROCHLORIDE 1
7602871 1017027843 C DARIFENACIN (EMSELEX) (DARIFENACIN) 2
7602871 1017027849 C SINEMET DEPOT (LEVODOPA) 2
7602871 1017027854 C COZAAR COMP (HYZAAR) 2
7602871 1016981754 PS OMNISCAN 1 PARENTERAL 20 ML, SINGLE DOSE, REPORTED: PARENTERAL D D 020123
7602871 1017027842 C LANSOPRAZOLE 1
7602871 1017027851 C VENOFER 1
7602871 1017027845 C CYANOCOBALAMIN 1
7602871 1017027852 C METOPROLOL TARTRATE 1
7602871 1017027837 C SIMVASTATIN 1
7602871 1017027847 C ASASANTIN RETARD (ACETYLSALICYLIC ACID) 2
7602871 1017027841 C CLONAZEPAM 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
7602871 1016981754 TRANSIENT ISCHAEMIC ATTACK

Outcome of event

Event ID OUTC COD
7602871 OT

Reactions reported

Event ID PT
7602871 HEMIANOPIA HETERONYMOUS

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

Event ID RPSR COD
7602871 FGN
7602871 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
7602871 1016981754 20110405 20110405