The Safety Rates Drug Report

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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
6856751 7536593 I 6856751-2 20090101 20100413 20100630 PER 1000013173 FOREST LABORATORIES, INC. 82 YR M N 20100610 CN 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
6856751 1014174924 PS BYSTOLIC 1 ORAL 5 MG (5 MG, 1 IN 1 D), ORAL D D 21742
6856751 1014391004 C DITROPAN XL (15 MILLIGRAM, TABLETS 2
6856751 1014391005 C BENICAR 1
6856751 1014391006 C NORVASC 1
6856751 1014391010 C LIPITOR (10 MILLIGRAM, TABLETS) 2
6856751 1014391011 C ZOLOFT 1
6856751 1014391012 C MULTIVITAMIN (TABLETS) 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
6856751 1014174924 HYPERTENSION

Outcome of event

no results found

Reactions reported

Event ID PT
6856751 NAUSEA

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

Event ID RPSR COD
6856751 CSM

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6856751 1014174924 20091001