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
127702631 12770263 1 I 20160510 20160922 20160922 PER US-DRREDDYS-DRL/USA/16/0079688 DR REDDYS 0.00 F Y 0.00000 20160922 CN US US

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
127702631 12770263 1 PS FLUCONAZOLE. FLUCONAZOLE 1 Oral U U UNKNOWN 76658 TABLET
127702631 12770263 2 C PROTONIX PANTOPRAZOLE SODIUM 1 Unknown 0
127702631 12770263 3 C LISINOPRIL. LISINOPRIL 1 Unknown 0
127702631 12770263 4 C GLIPIZIDE. GLIPIZIDE 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127702631 12770263 1 Urinary tract infection
127702631 12770263 2 Product used for unknown indication
127702631 12770263 3 Product used for unknown indication
127702631 12770263 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127702631 12770263 Blood glucose decreased
127702631 12770263 Diarrhoea
127702631 12770263 Headache
127702631 12770263 Palpitations

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
127702631 12770263 1 20160507 0