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
127504241 12750424 1 I 201605 20160516 20160915 20160915 PER US-ASTELLAS-2016US019433 ASTELLAS 54.10 YR M Y 0.00000 20160915 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
127504241 12750424 1 PS XTANDI ENZALUTAMIDE 1 Oral U 1543979PC 203415 160 MG CAPSULE QD
127504241 12750424 2 SS DOXYCYCLINE. DOXYCYCLINE 1 Unknown UNK UNK, UNKNOWN FREQ. U 0 FORMULATION UNKNOWN
127504241 12750424 3 C ASPIRIN. ASPIRIN 1 Unknown UNK UNK, UNKNOWN FREQ. U 0 FORMULATION UNKNOWN
127504241 12750424 4 C COENZYME Q10 UBIDECARENONE 1 Unknown UNK UNK, UNKNOWN FREQ. U 0 FORMULATION UNKNOWN
127504241 12750424 5 C DEXAMETHASONE. DEXAMETHASONE 1 Unknown UNK UNK, UNKNOWN FREQ. U 0 FORMULATION UNKNOWN
127504241 12750424 6 C OMEPRAZOLE. OMEPRAZOLE 1 Unknown UNK UNK, UNKNOWN FREQ. U 0 FORMULATION UNKNOWN
127504241 12750424 7 C POTASSIUM POTASSIUM 1 Unknown UNK UNK, UNKNOWN FREQ. U 0 FORMULATION UNKNOWN
127504241 12750424 8 C TURMERIC /01079601/ TURMERIC 1 Unknown UNK UNK, UNKNOWN FREQ. U 0 CAPSULE
127504241 12750424 9 C VITAMIN C ASCORBIC ACID 1 Unknown UNK UNK, UNKNOWN FREQ. U 0 TABLET
127504241 12750424 10 C VITAMIN D3 CHOLECALCIFEROL 1 Unknown UNK UNK, UNKNOWN FREQ. U 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127504241 12750424 1 Prostate cancer
127504241 12750424 2 Product used for unknown indication
127504241 12750424 3 Product used for unknown indication
127504241 12750424 4 Product used for unknown indication
127504241 12750424 5 Product used for unknown indication
127504241 12750424 6 Product used for unknown indication
127504241 12750424 7 Product used for unknown indication
127504241 12750424 8 Product used for unknown indication
127504241 12750424 9 Product used for unknown indication
127504241 12750424 10 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127504241 12750424 Fatigue
127504241 12750424 Hypersensitivity
127504241 12750424 Photosensitivity reaction
127504241 12750424 Rash

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
127504241 12750424 1 20160504 0