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
125528661 12552866 1 I 20160407 20160512 20160713 20160713 EXP PHHY2016IT067492 SANDOZ 82.17 YR F Y 0.00000 20160713 OT IT IT

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
125528661 12552866 1 PS AMOXICILLIN. AMOXICILLIN 1 Oral 1000 MG, QD Y 64076 1000 MG QD
125528661 12552866 2 C ONCO CARBIDE HYDROXYUREA 1 Oral 500 MG, UNK U 0 500 MG
125528661 12552866 3 C LOBIDIUR HYDROCHLOROTHIAZIDENEBIVOLOL HYDROCHLORIDE 1 Oral 1 DF, UNK U 0 1 DF

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125528661 12552866 1 Product used for unknown indication
125528661 12552866 2 Thrombocytosis
125528661 12552866 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125528661 12552866 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125528661 12552866 Presyncope
125528661 12552866 Pruritus
125528661 12552866 Rash
125528661 12552866 Vomiting

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125528661 12552866 1 20160407 20160407 0