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
6809365 6900758 F 6809365-4 20081107 20090311 20100630 EXP FR-ASTRAZENECA-2009CG00283 AZPRODUW00 23677 DY F Y 20100630 OT UNITED STATES

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
6809365 1014003063 PS CRESTOR 1 ORAL 21366
6809365 1014003064 SS FRACTAL 2 ORAL
6809365 1014003065 SS LESCOL 1 ORAL
6809365 1014003066 SS ZOCOR 1 ORAL
6809365 1014003067 SS EZETROL 2 ORAL
6809365 1014003068 SS LIPANTHYL 2 ORAL
6809365 1014003069 SS QUESTRAN 1 ORAL
6809365 1014003070 SS STATICONCEPT 2 ORAL
6809365 1014003071 C HOMEOPATHY 2
6809365 1014003072 C BONIVA 1
6809365 1014003073 C TELITHROMYCIN 2
6809365 1014003074 C LEKOVIT CA 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
6809365 1014003063 HYPERCHOLESTEROLAEMIA
6809365 1014003064 HYPERCHOLESTEROLAEMIA
6809365 1014003065 HYPERCHOLESTEROLAEMIA
6809365 1014003066 HYPERCHOLESTEROLAEMIA
6809365 1014003067 HYPERCHOLESTEROLAEMIA
6809365 1014003068 HYPERCHOLESTEROLAEMIA
6809365 1014003069 HYPERCHOLESTEROLAEMIA
6809365 1014003072 OSTEOPOROSIS

Outcome of event

Event ID OUTC COD
6809365 HO

Reactions reported

Event ID PT
6809365 ORGANISING PNEUMONIA

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
6809365 1014003063 20070101 20070601 5 MON
6809365 1014003064 20020101 20030101 1 YR
6809365 1014003065 20031201 20041101 11 MON
6809365 1014003066 20041201 20051001 10 MON
6809365 1014003067 20051101 20060301 4 MON
6809365 1014003068 20060301 20061201 9 MON
6809365 1014003069 20070701 20080501 10 MON
6809365 1014003070 20080501