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
119877634 11987763 4 F 20160805 20160202 20160808 EXP GB-ROCHE-1649192 ROCHE 0.00 F Y 0.00000 20160808 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
119877634 11987763 1 PS HERCEPTIN TRASTUZUMAB 1 Subcutaneous CYCLE 3, CYCLE 5 U 16F0605A 103792 600 MG SOLUTION FOR INJECTION
119877634 11987763 2 C TAMOXIFEN TAMOXIFEN 1 0
119877634 11987763 3 C RAMIPRIL. RAMIPRIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119877634 11987763 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
119877634 11987763 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119877634 11987763 Asthenia
119877634 11987763 Basal cell carcinoma
119877634 11987763 Constipation
119877634 11987763 Diarrhoea
119877634 11987763 Discomfort
119877634 11987763 Fatigue
119877634 11987763 Ill-defined disorder
119877634 11987763 Insomnia
119877634 11987763 Lacrimation increased
119877634 11987763 Onychoclasis
119877634 11987763 Pain
119877634 11987763 Pain in extremity
119877634 11987763 Rheumatoid arthritis
119877634 11987763 Wound haemorrhage
119877634 11987763 Wound secretion

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

no results found

Therapies reported

no results found