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
116446412 11644641 2 F 20150524 20160927 20151020 20160929 EXP PL-ASTRAZENECA-2015SE51792 ASTRAZENECA 23558.00 DY M Y 0.00000 20160930 MD PL PL

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
116446412 11644641 1 PS OLAPARIB OLAPARIB 1 Oral Y U 0 TABLET
116446412 11644641 2 SS OLAPARIB OLAPARIB 1 Oral Y U 0 TABLET
116446412 11644641 3 SS ABIRATERONE ABIRATERONE 1 Oral Y U 0 1000 MG TABLET QD
116446412 11644641 4 SS ABIRATERONE ABIRATERONE 1 Oral Y U 0 1000 MG TABLET QD
116446412 11644641 5 SS PREDNISONE. PREDNISONE 1 Oral 190 MG 0 5 MG TABLET BID
116446412 11644641 6 C ASPIRIN. ASPIRIN 1 Oral 0 75 MG QD
116446412 11644641 7 C CANDESARTANUM CILEXETILUM 2 Oral 0 32 MG QD
116446412 11644641 8 C FENOFIBRATUM 2 Oral 0 215 MG QD
116446412 11644641 9 C METFORMINI HYDROCHLORIDUM 2 Oral 0 250 MG BID
116446412 11644641 10 C LERCANIDIPINI HYDROCHLORIDUM 2 Oral 0 10 MG QD
116446412 11644641 11 C TORASEMIDUM 2 Oral 0 5 MG QD
116446412 11644641 12 C BISOPROLOLI FUMARAS 2 Oral 0 5 MG QD
116446412 11644641 13 C LEVOTHYROXINUM NATRICUM 2 Oral 0 150 MG QD
116446412 11644641 14 C VITRUM CALCIUM 2 Oral 0 1250 MG QD
116446412 11644641 15 C KATELIN SR 2 Oral 2 CAPSULES DAILY 0 CAPSULE
116446412 11644641 16 C ZOLEDRONIC ACID ACTAVIS ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 0 4 MG /month
116446412 11644641 17 C ZOLEDRONIC ACID ACTAVIS ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 0 4 MG /month

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116446412 11644641 1 Prostate cancer metastatic
116446412 11644641 2 Prostate cancer metastatic
116446412 11644641 3 Prostate cancer metastatic
116446412 11644641 4 Prostate cancer metastatic
116446412 11644641 5 Prostate cancer metastatic
116446412 11644641 6 Bone pain
116446412 11644641 7 Hypertension
116446412 11644641 8 Hyperlipidaemia
116446412 11644641 9 Diabetes mellitus
116446412 11644641 10 Hypertension
116446412 11644641 11 Hypertension
116446412 11644641 12 Hypertension
116446412 11644641 13 Hypothyroidism
116446412 11644641 14 Mineral supplementation
116446412 11644641 15 Mineral supplementation
116446412 11644641 16 Metastases to bone
116446412 11644641 17 Bone pain

Outcome of event

Event ID CASEID OUTC COD
116446412 11644641 HO
116446412 11644641 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
116446412 11644641 Febrile neutropenia

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
116446412 11644641 1 20150506 20150525 0
116446412 11644641 2 20150610 0
116446412 11644641 3 20150506 20150525 0
116446412 11644641 4 20150601 0
116446412 11644641 5 20150506 0