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
127356521 12735652 1 I 20160830 20160912 20160912 EXP GB-TEVA-689432ACC TEVA 0.00 F Y 0.00000 20160912 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
127356521 12735652 1 PS RAMIPRIL. RAMIPRIL 1 Unknown U U 77470
127356521 12735652 2 SS HERCEPTIN TRASTUZUMAB 1 Subcutaneous U U 0 600 MG SOLUTION FOR INJECTION
127356521 12735652 3 C LOSARTAN. LOSARTAN 1 Unknown 12.5 MILLIGRAM DAILY; 0 12.5 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127356521 12735652 1 Ejection fraction decreased
127356521 12735652 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127356521 12735652 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127356521 12735652 Abdominal pain upper
127356521 12735652 Anxiety
127356521 12735652 Asthenia
127356521 12735652 Constipation
127356521 12735652 Depression
127356521 12735652 Diarrhoea
127356521 12735652 Dizziness
127356521 12735652 Dry skin
127356521 12735652 Ejection fraction decreased
127356521 12735652 Erythema
127356521 12735652 Lacrimation increased
127356521 12735652 Lethargy
127356521 12735652 Muscle spasms
127356521 12735652 Myalgia
127356521 12735652 Neuropathy peripheral
127356521 12735652 Pain in extremity
127356521 12735652 Palpitations
127356521 12735652 Rhinorrhoea

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

no results found

Therapies reported

no results found