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
5117833 6139261 F 5117833-9 20060913 20060919 20060929 EXP HK-SANOFI-SYNTHELABO-F01200602006 SANOFI-SYNTHELABO M Y 20060929 OT

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
5117833 1007717871 C ADALAT 1 ORAL 40 MG
5117833 1007717872 C AMITRIPTYLINE HYDROCHLORIDE 1 ORAL 10 MG
5117833 1007717873 C ZOCOR 1 ORAL 10 MG
5117833 1007717874 C ZESTRIL 1 ORAL 10 MG
5117833 1007717875 SS MICARDIS 1 ORAL
5117833 1007717876 PS CLOPIDOGREL 1 ORAL 020839
5117833 1007717877 C CLOTRIMAZOLE 1 UNKNOWN

Indications of drugs used

Event ID DRUG SEQ INDI PT
5117833 1007717871 HYPERTENSION
5117833 1007717872 HYPOAESTHESIA
5117833 1007717873 HYPERLIPIDAEMIA
5117833 1007717874 HYPERTENSION
5117833 1007717876 CEREBROVASCULAR ACCIDENT
5117833 1007717877 FUNGAL SKIN INFECTION

Outcome of event

Event ID OUTC COD
5117833 HO

Reactions reported

Event ID PT
5117833 GASTRITIS EROSIVE
5117833 OESOPHAGEAL ULCER

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
5117833 1007717871 20060515
5117833 1007717872 20041103
5117833 1007717874 20050214
5117833 1007717875 20051007
5117833 1007717876 20051017
5117833 1007717877 20060907