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
127310322 12731032 2 F 20160915 20160912 20160926 EXP GB-MHRA-ADR 23496037 GB-ACCORD-043770 ACCORD 0.00 F Y 0.00000 20160926 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
127310322 12731032 1 PS RAMIPRIL. RAMIPRIL 1 Unknown Y 202392
127310322 12731032 2 SS HERCEPTIN TRASTUZUMAB 1 Subcutaneous U 0 600 MG
127310322 12731032 3 C LOSARTAN. LOSARTAN 1 Unknown 0 12.5 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127310322 12731032 1 Ejection fraction decreased
127310322 12731032 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127310322 12731032 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127310322 12731032 Abdominal pain upper
127310322 12731032 Anxiety
127310322 12731032 Asthenia
127310322 12731032 Constipation
127310322 12731032 Depression
127310322 12731032 Diarrhoea
127310322 12731032 Dizziness
127310322 12731032 Dry skin
127310322 12731032 Ejection fraction decreased
127310322 12731032 Erythema
127310322 12731032 Lacrimation increased
127310322 12731032 Lethargy
127310322 12731032 Muscle spasms
127310322 12731032 Myalgia
127310322 12731032 Neuropathy peripheral
127310322 12731032 Palpitations
127310322 12731032 Rhinorrhoea

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

no results found

Therapies reported

no results found