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
126293151 12629315 1 I 20160726 20160808 20160808 EXP GB-AUROBINDO-AUR-APL-2016-09870 AUROBINDO 0.00 F Y 0.00000 20160808 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
126293151 12629315 1 PS RAMIPRIL. RAMIPRIL 1 Unknown U U 91604
126293151 12629315 2 SS HERCEPTIN TRASTUZUMAB 1 Subcutaneous 600 MG, UNK U U 0 600 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126293151 12629315 1 Product used for unknown indication
126293151 12629315 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126293151 12629315 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126293151 12629315 Constipation
126293151 12629315 Dry skin
126293151 12629315 Fatigue
126293151 12629315 Hyperaesthesia
126293151 12629315 Hyperhidrosis
126293151 12629315 Insomnia
126293151 12629315 Malaise
126293151 12629315 Muscle spasms
126293151 12629315 Nausea
126293151 12629315 Oedema peripheral
126293151 12629315 Pain
126293151 12629315 Paraesthesia
126293151 12629315 Sleep disorder
126293151 12629315 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