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
127253401 12725340 1 I 201606 20160829 20160908 20160908 EXP US-ELI_LILLY_AND_COMPANY-US201608014435 ELI LILLY AND CO 79.66 YR M Y 0.00000 20160907 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
127253401 12725340 1 PS CIALIS TADALAFIL 1 Oral 20 MG, QD N U C519455A 21368 20 MG TABLET QD
127253401 12725340 2 SS CIALIS TADALAFIL 1 Oral 5 MG, EACH MORNING N U 21368 5 MG TABLET QD
127253401 12725340 3 SS CIALIS TADALAFIL 1 Oral 20 MG, EACH EVENING N U 21368 20 MG TABLET QD
127253401 12725340 4 SS CIALIS TADALAFIL 1 Oral 20 MG, PRN N U 21368 20 MG TABLET
127253401 12725340 5 C DIOVAN VALSARTAN 1 0
127253401 12725340 6 C NIFEDIPINE. NIFEDIPINE 1 0
127253401 12725340 7 C LIPITOR ATORVASTATIN CALCIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127253401 12725340 1 Erectile dysfunction

Outcome of event

Event ID CASEID OUTC COD
127253401 12725340 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127253401 12725340 Drug ineffective
127253401 12725340 Dyspepsia
127253401 12725340 Incorrect dose administered
127253401 12725340 Intestinal obstruction

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
127253401 12725340 1 201606 0
127253401 12725340 4 20160827 0