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
126269861 12626986 1 I 20160726 20160805 20160805 EXP GB-TEVA-681055ACC TEVA 0.00 F Y 0.00000 20160805 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
126269861 12626986 1 PS RAMIPRIL. RAMIPRIL 1 Unknown U U 77470
126269861 12626986 2 SS HERCEPTIN TRASTUZUMAB 1 Subcutaneous U U 0 600 MG SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126269861 12626986 1 Product used for unknown indication
126269861 12626986 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126269861 12626986 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126269861 12626986 Constipation
126269861 12626986 Dry skin
126269861 12626986 Fatigue
126269861 12626986 Hyperaesthesia
126269861 12626986 Hyperhidrosis
126269861 12626986 Insomnia
126269861 12626986 Malaise
126269861 12626986 Muscle spasms
126269861 12626986 Nausea
126269861 12626986 Oedema peripheral
126269861 12626986 Pain
126269861 12626986 Paraesthesia
126269861 12626986 Sleep disorder
126269861 12626986 Urinary tract infection

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

no results found

Therapies reported

no results found