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
4959787 6016863 I 4959787-1 20060324 20060331 EXP IT-BOEHRINGER INGELHEIM PHARMACEUTICALS, INC.-2006-DE-01572GD BOEHRINGER INGELHEIM PHARMACEUTICALS, INC. Y 20060331

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
4959787 1007117979 PS TAMSULOSIN HCL 1 20579
4959787 1007117980 SS AESCULUS HIPPOCASTANUM 2
4959787 1007117981 SS DICLOFENAC 2
4959787 1007117982 SS OMEPRAZOLE 1
4959787 1007117983 SS LEVOFLOXACIN 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
4959787 1007117979 CALCULUS URETERIC
4959787 1007117980 CALCULUS URETERIC
4959787 1007117981 CALCULUS URETERIC

Outcome of event

Event ID OUTC COD
4959787 HO

Reactions reported

Event ID PT
4959787 ABDOMINAL PAIN
4959787 DISEASE RECURRENCE
4959787 HYPOTENSION

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

no results found

Therapies reported

no results found