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
126257351 12625735 1 I 20160726 20160805 20160805 EXP GB-PFIZER INC-2016368637 PFIZER 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
126257351 12625735 1 PS RAMIPRIL. RAMIPRIL 1 Unknown UNK U 19901
126257351 12625735 2 SS HERCEPTIN TRASTUZUMAB 1 Subcutaneous 600 MG, CYCLIC U 0 600 MG INJECTION

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126257351 12625735 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126257351 12625735 Constipation
126257351 12625735 Dry skin
126257351 12625735 Fatigue
126257351 12625735 Hyperaesthesia
126257351 12625735 Hyperhidrosis
126257351 12625735 Insomnia
126257351 12625735 Malaise
126257351 12625735 Muscle spasms
126257351 12625735 Nausea
126257351 12625735 Oedema peripheral
126257351 12625735 Pain
126257351 12625735 Paraesthesia
126257351 12625735 Sleep disorder
126257351 12625735 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