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
125971791 12597179 1 I 20160627 0 20160726 20160726 DIR 68.00 YR F N 163.00000 LBS 20160725 N 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
125971791 12597179 1 PS AZITHROMYCIN ANHYDROUS. AZITHROMYCIN ANHYDROUS 1 Oral 6 TABLET(S) ONCE A DAY TAKEN BY MOUTH Y D 1505009255 0 6 DF COATED TABLET QD
125971791 12597179 3 C METOPROLOL TART METOPROLOL TARTRATE 1 0
125971791 12597179 5 C POTACHLORIDE 2 0
125971791 12597179 7 C RANITIDINE. RANITIDINE 1 0
125971791 12597179 9 C HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 0
125971791 12597179 11 C LOSARTAN POTASSIUM. LOSARTAN POTASSIUM 1 0
125971791 12597179 13 C VENTOLIN HFA (INHALER) 2 0
125971791 12597179 15 C VITAMIN B12 CYANOCOBALAMIN 1 0
125971791 12597179 17 C VITAMIN D3 CHOLECALCIFEROL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125971791 12597179 1 Cough
125971791 12597179 1 Pharyngitis streptococcal

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125971791 12597179 Cold sweat
125971791 12597179 Diarrhoea
125971791 12597179 Dizziness
125971791 12597179 Loss of consciousness
125971791 12597179 Malaise

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
125971791 12597179 1 20160627 20160627 0