The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
117804962 11780496 2 F 20150804 20151126 20160726 PER IR-GLENMARK PHARMACEUTICALS INC, USA.-2015GMK018953 GLENMARK EHSANI-ARDAKANI M J, SEDAGHAT M, ESLAMI G, SHALMANI H M.. THE HELICOBACTER PYLORI ERADICATION IN THE GROUP RECEIVING STANDARD -DOSE AND GROUP CONTINUE TAKING AMOXICILLIN FOR 4 WEEKS; A CLINICAL TRIAL STUDY. GASTROENTEROLOGY AND HEPATOLOGY. 2015;8(SUPPL.1):S54-S59 0.00 Y 0.00000 20160726 OT IR IR

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
117804962 11780496 1 PS OMEPRAZOLE. OMEPRAZOLE 1 20 MG, BID FOR TWO WEEKS U 91672 20 MG BID
117804962 11780496 2 SS AMOXICILLIN. AMOXICILLIN 1 1 G, BID FOR TWO WEEKS U 0 1 G BID
117804962 11780496 3 SS AMOXICILLIN. AMOXICILLIN 1 1 G, BID FOR FOUR WEEKS U 0 1 G BID
117804962 11780496 4 SS CLARITHROMYCIN. CLARITHROMYCIN 1 500 MG, BID FOR TWO WEEKS U 0 500 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117804962 11780496 1 Helicobacter infection
117804962 11780496 2 Helicobacter infection
117804962 11780496 4 Helicobacter infection

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
117804962 11780496 Abdominal distension
117804962 11780496 Dysgeusia
117804962 11780496 Off label use

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

no results found

Therapies reported

no results found