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
126197311 12619731 1 I 20160726 20160803 20160803 EXP PHHY2016GB103051 SANDOZ 0.00 F Y 0.00000 20160803 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
126197311 12619731 1 PS RAMIPRIL. RAMIPRIL 1 Unknown U 77514
126197311 12619731 2 SS HERCEPTIN TRASTUZUMAB 1 Subcutaneous 600 MG, UNK U 0 600 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126197311 12619731 1 Product used for unknown indication
126197311 12619731 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126197311 12619731 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126197311 12619731 Constipation
126197311 12619731 Dry skin
126197311 12619731 Fatigue
126197311 12619731 Hyperaesthesia
126197311 12619731 Hyperhidrosis
126197311 12619731 Insomnia
126197311 12619731 Malaise
126197311 12619731 Muscle spasms
126197311 12619731 Nausea
126197311 12619731 Oedema peripheral
126197311 12619731 Pain
126197311 12619731 Paraesthesia
126197311 12619731 Sleep disorder
126197311 12619731 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