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
125955191 12595519 1 I 20160704 20160720 20160726 20160726 PER PHEH2016US018462 NOVARTIS 49.86 YR F Y 108.80000 KG 20160726 MD 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
125955191 12595519 1 PS ESTRADIOL. ESTRADIOL 1 Unknown UNK 79622 19081 PATCH
125955191 12595519 2 C VITAMIN D CHOLECALCIFEROL 1 Unknown U 0
125955191 12595519 3 C FLAXSEED FLAX SEED 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125955191 12595519 1 Product used for unknown indication
125955191 12595519 2 Product used for unknown indication
125955191 12595519 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125955191 12595519 Body temperature decreased
125955191 12595519 Pyrexia
125955191 12595519 Rash
125955191 12595519 Rash generalised
125955191 12595519 Rash macular
125955191 12595519 Urticaria

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
125955191 12595519 1 201603 0