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
126548971 12654897 1 I 20160727 20160816 20160816 PER US-ELI_LILLY_AND_COMPANY-US201607013078 ELI LILLY AND CO 0.00 M Y 0.00000 20160816 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
126548971 12654897 1 PS CIALIS TADALAFIL 1 Unknown 5 MG, QD U A971131A 21368 5 MG TABLET QD
126548971 12654897 2 SS CIALIS TADALAFIL 1 Unknown 20 MG, PRN U C437434A 21368 20 MG TABLET
126548971 12654897 3 SS CIALIS TADALAFIL 1 Unknown 5 MG, QD U 21368 5 MG TABLET QD
126548971 12654897 4 SS CIALIS TADALAFIL 1 Unknown 20 MG, PRN U 21368 20 MG TABLET
126548971 12654897 5 C ASA ASPIRIN 1 0
126548971 12654897 6 C VITAMIIN C ASCORBIC ACID 1 0
126548971 12654897 7 C VITAMIN D CHOLECALCIFEROL 1 0
126548971 12654897 8 C PRAVASTATIN. PRAVASTATIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126548971 12654897 1 Erectile dysfunction

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126548971 12654897 Abdominal discomfort
126548971 12654897 Back pain
126548971 12654897 Diarrhoea
126548971 12654897 Drug ineffective
126548971 12654897 Expired product administered
126548971 12654897 Vomiting

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
126548971 12654897 2 201602 0
126548971 12654897 3 201607 0
126548971 12654897 4 20160723 0