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
127183221 12718322 1 I 20160830 20160906 20160906 EXP PHHY2016GB119152 SANDOZ 0.00 F Y 0.00000 20160906 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
127183221 12718322 1 PS RAMIPRIL. RAMIPRIL 1 Unknown U U 77514
127183221 12718322 2 SS HERCEPTIN TRASTUZUMAB 1 Subcutaneous 600 MG U U 0 600 MG
127183221 12718322 3 C LOSARTAN. LOSARTAN 1 Unknown 12.5 MG, QD U 0 12.5 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127183221 12718322 1 Ejection fraction decreased
127183221 12718322 2 Product used for unknown indication
127183221 12718322 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127183221 12718322 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127183221 12718322 Abdominal pain upper
127183221 12718322 Anxiety
127183221 12718322 Asthenia
127183221 12718322 Constipation
127183221 12718322 Depression
127183221 12718322 Diarrhoea
127183221 12718322 Dizziness
127183221 12718322 Dry skin
127183221 12718322 Ejection fraction decreased
127183221 12718322 Erythema
127183221 12718322 Lacrimation increased
127183221 12718322 Lethargy
127183221 12718322 Muscle spasms
127183221 12718322 Myalgia
127183221 12718322 Neuropathy peripheral
127183221 12718322 Pain in extremity
127183221 12718322 Palpitations
127183221 12718322 Rhinorrhoea

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

no results found

Therapies reported

no results found