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
127556761 12755676 1 I 2016 20160830 20160916 20160916 PER US-ELI_LILLY_AND_COMPANY-US201609000421 ELI LILLY AND CO 0.00 M Y 0.00000 20160916 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
127556761 12755676 1 PS CIALIS TADALAFIL 1 Oral 5 MG, QD 21368 5 MG TABLET QD
127556761 12755676 2 C CRESTOR ROSUVASTATIN CALCIUM 1 Unknown UNK, UNKNOWN U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127556761 12755676 1 Benign prostatic hyperplasia
127556761 12755676 2 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127556761 12755676 Acarodermatitis
127556761 12755676 Dermatitis
127556761 12755676 Drug hypersensitivity
127556761 12755676 Erythema
127556761 12755676 Inflammation
127556761 12755676 Rash pruritic
127556761 12755676 Scab
127556761 12755676 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
127556761 12755676 1 201604 0