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
126287571 12628757 1 I 20160726 20160808 20160808 EXP GB-MHRA-ADR 23580555 GB-ACCORD-042830 ACCORD 0.00 F Y 0.00000 20160808 CN 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
126287571 12628757 1 PS RAMIPRIL. RAMIPRIL 1 Unknown U 202392
126287571 12628757 2 SS HERCEPTIN TRASTUZUMAB 1 Subcutaneous U 0 600 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126287571 12628757 1 Product used for unknown indication
126287571 12628757 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126287571 12628757 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126287571 12628757 Constipation
126287571 12628757 Dry skin
126287571 12628757 Fatigue
126287571 12628757 Hyperaesthesia
126287571 12628757 Hyperhidrosis
126287571 12628757 Insomnia
126287571 12628757 Malaise
126287571 12628757 Muscle spasms
126287571 12628757 Nausea
126287571 12628757 Oedema peripheral
126287571 12628757 Pain
126287571 12628757 Paraesthesia
126287571 12628757 Sleep disorder
126287571 12628757 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