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
125033053 12503305 3 F 20160406 20160825 20160628 20160908 EXP GB-AUROBINDO-AUR-APL-2016-07945 AUROBINDO 67.00 YR F Y 80.00000 KG 20160908 CN GB GB

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
125033053 12503305 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Unknown U U 77859
125033053 12503305 2 SS CLEXANE ENOXAPARIN SODIUM 1 Subcutaneous 6 WEEK COURSE ENDED AFTER 32 DAYS 5SA23(12/16) 5SA74(01/17) 5SF52(03/17) 5SL64(08/17) 5SK16 (05/17). 2395 MG Y U 5SK16 0 120 MG SOLUTION FOR INJECTION QD
125033053 12503305 3 SS CLEXANE ENOXAPARIN SODIUM 1 2395 MG Y U 0 SOLUTION FOR INJECTION
125033053 12503305 4 C ADCAL D3 CALCIUM CARBONATECHOLECALCIFEROL 1 Unknown UNK U 0
125033053 12503305 5 C LETROZOLE. LETROZOLE 1 Unknown U 0
125033053 12503305 6 C OMEPRAZOLE. OMEPRAZOLE 1 Unknown U 0
125033053 12503305 7 C ZOMORPH MORPHINE SULFATE 1 Unknown U 0
125033053 12503305 8 C PERJETA PERTUZUMAB 1 Unknown U 0
125033053 12503305 9 C HERCEPTIN TRASTUZUMAB 1 Unknown 1 DF, UNK U 0 1 DF
125033053 12503305 10 C PERTUZUMAB PERTUZUMAB 1 Unknown 1 DF, UNK U 0 1 DF
125033053 12503305 11 C DENOSUMAB DENOSUMAB 1 Unknown 1 DF, UNK U 0 1 DF INJECTION
125033053 12503305 12 C DOCETAXEL. DOCETAXEL 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125033053 12503305 1 Antibiotic therapy
125033053 12503305 2 Peripheral embolism
125033053 12503305 3 Peripheral embolism
125033053 12503305 4 Product used for unknown indication
125033053 12503305 5 Product used for unknown indication
125033053 12503305 6 Product used for unknown indication
125033053 12503305 7 Product used for unknown indication
125033053 12503305 8 Product used for unknown indication
125033053 12503305 9 Breast cancer stage IV
125033053 12503305 10 Breast cancer stage IV
125033053 12503305 11 Bone disorder
125033053 12503305 12 Breast cancer stage IV

Outcome of event

Event ID CASEID OUTC COD
125033053 12503305 LT
125033053 12503305 OT
125033053 12503305 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125033053 12503305 Blister
125033053 12503305 Burning sensation
125033053 12503305 Dermatitis
125033053 12503305 Erythema multiforme
125033053 12503305 Pain
125033053 12503305 Protein deficiency
125033053 12503305 Rash erythematous
125033053 12503305 Scab
125033053 12503305 Skin erosion
125033053 12503305 Skin haemorrhage
125033053 12503305 Tachycardia

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
125033053 12503305 2 20160317 20160417 0
125033053 12503305 4 20151016 0
125033053 12503305 12 20160210 0