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
6810392 7323613 F 6810392-1 20091116 20100616 20100630 EXP PHHY2010JP13839 NOVARTIS PHARMACEUTICAL CORPORATION 58 YR M Y 46 KG 20100630 MD 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
6810392 1014007692 PS DIOVAN 1 ORAL 40 MG, QD 021283
6810392 1014007693 SS DIOVAN 1 ORAL 80 MG, QD 021283
6810392 1014007694 SS VOLTAREN 1 25 MG DAILY
6810392 1014007695 C NATRIX 2 ORAL 1 MG, UNK
6810392 1014007696 C NORVASC 1 ORAL 5 MG, UNK
6810392 1014007697 C NORVASC 1 ORAL 10 MG, UNK
6810392 1014007698 C ZANTAC 1 ORAL 150 MG, UNK
6810392 1014007699 C ZANTAC 1 ORAL 300 MG, UNK
6810392 1014007700 C OMEPRAL 2 ORAL 20 MG DAILY

Indications of drugs used

Event ID DRUG SEQ INDI PT
6810392 1014007692 HYPERTENSION
6810392 1014007694 PAIN

Outcome of event

Event ID OUTC COD
6810392 HO
6810392 OT

Reactions reported

Event ID PT
6810392 BLOOD PRESSURE DIASTOLIC DECREASED
6810392 BLOOD PRESSURE SYSTOLIC INCREASED
6810392 GASTRIC ULCER HAEMORRHAGE
6810392 GASTROINTESTINAL HAEMORRHAGE

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
6810392 1014007692 20090912 20091211 91 DAY
6810392 1014007693 20091212
6810392 1014007694 20090903 20091106 65 DAY
6810392 1014007695 20090918
6810392 1014007696 20091020
6810392 1014007697 20091020
6810392 1014007698 20020425
6810392 1014007699 20020425
6810392 1014007700 20100112 20100211 31 DAY