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
118709339 11870933 9 F 20160509 20160624 20151228 20160701 EXP PHHY2015GB164836 SANDOZ 53.00 YR F Y 0.00000 20160701 OT 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
118709339 11870933 1 PS CARBOPLATIN. CARBOPLATIN 1 Unknown UNK U 76959
118709339 11870933 2 SS CARBOPLATIN. CARBOPLATIN 1 Unknown CYCLE 10 U 76959
118709339 11870933 3 SS GEMCITABINE GEMCITABINEGEMCITABINE HYDROCHLORIDE 1 Unknown U 0
118709339 11870933 4 SS GEMCITABINE GEMCITABINEGEMCITABINE HYDROCHLORIDE 1 Unknown U 0
118709339 11870933 5 SS GEMCITABINE GEMCITABINEGEMCITABINE HYDROCHLORIDE 1 Unknown CYCLE 10 U 0
118709339 11870933 6 SS CHLORHEXIDINE CHLORHEXIDINE 1 Unknown U 0
118709339 11870933 7 SS CHLORHEXIDINE CHLORHEXIDINE 1 Unknown U 0
118709339 11870933 8 SS HERCEPTIN TRASTUZUMAB 1 Subcutaneous 600 MG U 0 600 MG
118709339 11870933 9 SS HERCEPTIN TRASTUZUMAB 1 Subcutaneous U 0
118709339 11870933 10 SS HERCEPTIN TRASTUZUMAB 1 Subcutaneous U 0 600 MG
118709339 11870933 11 C VINORELBINE VINORELBINEVINORELBINE TARTRATE 1 Oral U 0
118709339 11870933 12 C VINORELBINE VINORELBINEVINORELBINE TARTRATE 1 Oral U 0
118709339 11870933 13 C VINORELBINE VINORELBINEVINORELBINE TARTRATE 1 Oral U 0
118709339 11870933 14 C VINORELBINE VINORELBINEVINORELBINE TARTRATE 1 Oral U 0
118709339 11870933 15 C VINORELBINE VINORELBINEVINORELBINE TARTRATE 1 Oral U 0
118709339 11870933 16 C VINORELBINE VINORELBINEVINORELBINE TARTRATE 1 Oral U 0
118709339 11870933 17 C GRANISETRON GRANISETRON 1 Unknown U 0
118709339 11870933 18 C GRANISETRON GRANISETRON 1 Unknown U 0
118709339 11870933 19 C NEULASTA PEGFILGRASTIM 1 Unknown U 0
118709339 11870933 20 C NEULASTA PEGFILGRASTIM 1 Unknown U 0
118709339 11870933 21 C DEXAMETHASONE. DEXAMETHASONE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118709339 11870933 1 Product used for unknown indication
118709339 11870933 3 Product used for unknown indication
118709339 11870933 6 Product used for unknown indication
118709339 11870933 8 Product used for unknown indication
118709339 11870933 11 Product used for unknown indication
118709339 11870933 17 Product used for unknown indication
118709339 11870933 19 Product used for unknown indication
118709339 11870933 21 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
118709339 11870933 HO
118709339 11870933 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
118709339 11870933 Allergy to chemicals
118709339 11870933 Anaemia
118709339 11870933 Blood creatinine increased
118709339 11870933 Breast cancer metastatic
118709339 11870933 Constipation
118709339 11870933 Cough
118709339 11870933 Diarrhoea
118709339 11870933 Dysgeusia
118709339 11870933 Dysphonia
118709339 11870933 Fatigue
118709339 11870933 Haemoglobin decreased
118709339 11870933 Hyperaesthesia
118709339 11870933 Hypokinesia
118709339 11870933 Limb discomfort
118709339 11870933 Lymphoedema
118709339 11870933 Musculoskeletal disorder
118709339 11870933 Nausea
118709339 11870933 Neuralgia
118709339 11870933 Neuropathy peripheral
118709339 11870933 Oedema
118709339 11870933 Pain in extremity
118709339 11870933 Paraesthesia
118709339 11870933 Pyrexia
118709339 11870933 Rhinorrhoea
118709339 11870933 Sensory loss
118709339 11870933 Vomiting
118709339 11870933 Wound
118709339 11870933 Wound haemorrhage
118709339 11870933 Wound secretion

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found