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
126467511 12646751 1 I 20160801 20160812 20160812 EXP GB-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-121943 RANBAXY 57.00 YR M Y 0.00000 20160812 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
126467511 12646751 1 SS Calcium folinat LEUCOVORIN CALCIUM 1 Unknown U U 0
126467511 12646751 2 PS DEXAMETHASONE. DEXAMETHASONE 1 Unknown U U 84764
126467511 12646751 3 SS Irinotecan IRINOTECAN 1 Unknown U U 0
126467511 12646751 4 SS Ondansetron ONDANSETRON 1 Unknown U U 0
126467511 12646751 5 SS TRAMADOL. TRAMADOL 1 Unknown U U 0
126467511 12646751 6 SS 5-FU FLUOROURACIL 1 Unknown CYCLE 8 DAY 1 U U 0
126467511 12646751 7 SS APREPITANT. APREPITANT 1 Unknown U U 0
126467511 12646751 8 SS ATROPINE. ATROPINE 1 Unknown U U 0
126467511 12646751 9 SS AVASTIN BEVACIZUMAB 1 Unknown U U 0
126467511 12646751 10 SS BEVACIZUMAB BEVACIZUMAB 1 Unknown U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126467511 12646751 1 Product used for unknown indication
126467511 12646751 2 Product used for unknown indication
126467511 12646751 3 Product used for unknown indication
126467511 12646751 4 Product used for unknown indication
126467511 12646751 5 Product used for unknown indication
126467511 12646751 6 Product used for unknown indication
126467511 12646751 7 Product used for unknown indication
126467511 12646751 8 Product used for unknown indication
126467511 12646751 9 Product used for unknown indication
126467511 12646751 10 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126467511 12646751 OT
126467511 12646751 HO
126467511 12646751 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126467511 12646751 Alopecia
126467511 12646751 Arthropathy
126467511 12646751 Change of bowel habit
126467511 12646751 Decreased appetite
126467511 12646751 Diarrhoea
126467511 12646751 Emotional disorder
126467511 12646751 Fatigue
126467511 12646751 Gait disturbance
126467511 12646751 Hypertension
126467511 12646751 Ill-defined disorder
126467511 12646751 Mouth ulceration
126467511 12646751 Muscular weakness
126467511 12646751 Oral pain
126467511 12646751 Pain
126467511 12646751 Pyrexia
126467511 12646751 Rhinorrhoea
126467511 12646751 Stoma site pain

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

no results found

Therapies reported

no results found