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
127541651 12754165 1 I 20160520 20160915 20160916 20160916 EXP GB-ROCHE-1831245 ROCHE 0.00 F Y 0.00000 20160916 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
127541651 12754165 1 PS HERCEPTIN TRASTUZUMAB 1 Subcutaneous UNK U U 103792 600 MG SOLUTION FOR INJECTION
127541651 12754165 2 SS RAMIPRIL. RAMIPRIL 1 Unknown UNK Y U 0
127541651 12754165 3 C LOSARTAN. LOSARTAN 1 Unknown 12.5 MG, 1X/DAY 0 12.5 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127541651 12754165 1 Product used for unknown indication
127541651 12754165 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127541651 12754165 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127541651 12754165 Abdominal pain upper
127541651 12754165 Anxiety
127541651 12754165 Asthenia
127541651 12754165 Constipation
127541651 12754165 Depression
127541651 12754165 Diarrhoea
127541651 12754165 Dizziness
127541651 12754165 Dry skin
127541651 12754165 Ejection fraction decreased
127541651 12754165 Erythema
127541651 12754165 Lacrimation increased
127541651 12754165 Lethargy
127541651 12754165 Muscle spasms
127541651 12754165 Myalgia
127541651 12754165 Neuropathy peripheral
127541651 12754165 Pain in extremity
127541651 12754165 Palpitations
127541651 12754165 Rhinorrhoea

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

no results found

Therapies reported

no results found