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
127781731 12778173 1 I 20160520 20160915 20160925 20160925 EXP PHHY2016GB127938 SANDOZ 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
127781731 12778173 1 PS RAMIPRIL. RAMIPRIL 1 Unknown Y U 77514
127781731 12778173 2 SS HERCEPTIN TRASTUZUMAB 1 Subcutaneous 600 MG U U 0 600 MG
127781731 12778173 3 C LOSARTAN. LOSARTAN 1 Unknown 12.5 MG, QD, 12.5 MG, 1X/DAY U 0 12.5 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127781731 12778173 1 Product used for unknown indication
127781731 12778173 2 Product used for unknown indication
127781731 12778173 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127781731 12778173 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127781731 12778173 Abdominal pain upper
127781731 12778173 Anxiety
127781731 12778173 Asthenia
127781731 12778173 Constipation
127781731 12778173 Depression
127781731 12778173 Diarrhoea
127781731 12778173 Dizziness
127781731 12778173 Dry skin
127781731 12778173 Ejection fraction decreased
127781731 12778173 Erythema
127781731 12778173 Lacrimation increased
127781731 12778173 Lethargy
127781731 12778173 Muscle spasms
127781731 12778173 Myalgia
127781731 12778173 Neuropathy peripheral
127781731 12778173 Pain in extremity
127781731 12778173 Palpitations
127781731 12778173 Rhinorrhoea

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

no results found

Therapies reported

no results found