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
7790566 8139544 F 7790566-6 20110720 20110922 20110930 EXP JP-SHIRE-ALL1-2011-03335 SHIRE DEVELOPMENT INC 80 YR F Y 20110930 CN JAPAN

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
7790566 1017682739 PS FOSRENOL 1 ORAL 2250 MG, UNKNOWN 021468
7790566 1017682743 C OLOPATADINE HCL 1 ORAL 10 MG, UNKNOWN
7790566 1017682742 C METROC 2 ORAL 20 MG, UNKNOWN
7790566 1017682740 C OMERAP 2 ORAL 200 MG, UNKNOWN
7790566 1017682741 C DOPS 2 ORAL 400 MG, UNKNOWN
7790566 1017682744 C LAMISIL 1 ORAL 125 MG, UNKNOWN

Indications of drugs used

Event ID DRUG SEQ INDI PT
7790566 1017682739 HYPERPHOSPHATAEMIA
7790566 1017682743 PRURITUS
7790566 1017682742 HYPOTENSION
7790566 1017682740 GASTROOESOPHAGEAL REFLUX DISEASE
7790566 1017682741 HYPOTENSION
7790566 1017682744 ONYCHOMYCOSIS

Outcome of event

Event ID OUTC COD
7790566 HO

Reactions reported

Event ID PT
7790566 C-REACTIVE PROTEIN INCREASED
7790566 ABDOMINAL PAIN LOWER

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
7790566 1017682739 20110427 20110722 87 DAY
7790566 1017682743 20060905
7790566 1017682742 20080402
7790566 1017682740 20051115
7790566 1017682741 20080402
7790566 1017682744 20100903