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
126177891 12617789 1 I 20160722 20160803 20160803 PER US-ASTRAZENECA-2016SE81172 ASTRAZENECA 0.00 F Y 68.00000 KG 20160803 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
126177891 12617789 1 PS CRESTOR ROSUVASTATIN CALCIUM 1 Oral 21366 10 MG TABLET QD
126177891 12617789 2 C PROBIOTIC PROBIOTICS NOS 1 0 QD
126177891 12617789 3 C VITAMIN D3 CHOLECALCIFEROL 1 5000 ,DAILY 0
126177891 12617789 4 C COQ10 UBIDECARENONE 1 0 200 MG QD
126177891 12617789 5 C MULTIVITAMIN VITAMINS 1 0 QD
126177891 12617789 6 C HAIR VITAMIN 2 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126177891 12617789 1 Blood cholesterol increased
126177891 12617789 2 Nutritional supplementation
126177891 12617789 3 Nutritional supplementation
126177891 12617789 4 Nutritional supplementation
126177891 12617789 5 Nutritional supplementation
126177891 12617789 6 Nutritional supplementation

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126177891 12617789 Adverse event
126177891 12617789 Weight increased

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

no results found

Therapies reported

no results found