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
126338831 12633883 1 I 20160729 20160809 20160809 EXP GB-PFIZER INC-2016369498 PFIZER 57.00 YR M Y 0.00000 20160809 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
126338831 12633883 1 SS FLUOROURACIL. FLUOROURACIL 1 Unknown UNK (CYCLE 8 DAY 1) U 0
126338831 12633883 2 PS IRINOTECAN HCL IRINOTECAN HYDROCHLORIDE 1 Unknown UNK (MODIFIED DE GRAMONT) U 20571
126338831 12633883 3 SS APREPITANT. APREPITANT 1 Unknown UNK U 0
126338831 12633883 4 SS ATROPINE. ATROPINE 1 Unknown UNK U 0
126338831 12633883 5 SS AVASTIN BEVACIZUMAB 1 Unknown UNK U 0
126338831 12633883 6 SS CALCIUM FOLINATE LEUCOVORIN CALCIUM 1 Unknown UNK U 0
126338831 12633883 7 SS DEXAMETHASONE. DEXAMETHASONE 1 Unknown UNK U 0
126338831 12633883 8 SS ONDANSETRON ONDANSETRON 1 Unknown UNK U 0
126338831 12633883 9 SS TRAMADOL. TRAMADOL 1 Unknown UNK U 0
126338831 12633883 10 SS BEVACIZUMAB BEVACIZUMAB 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126338831 12633883 1 Product used for unknown indication
126338831 12633883 3 Product used for unknown indication
126338831 12633883 4 Product used for unknown indication
126338831 12633883 5 Product used for unknown indication
126338831 12633883 6 Product used for unknown indication
126338831 12633883 7 Product used for unknown indication
126338831 12633883 8 Product used for unknown indication
126338831 12633883 9 Product used for unknown indication
126338831 12633883 10 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126338831 12633883 OT
126338831 12633883 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126338831 12633883 Alopecia
126338831 12633883 Arthropathy
126338831 12633883 Change of bowel habit
126338831 12633883 Decreased appetite
126338831 12633883 Diarrhoea
126338831 12633883 Emotional disorder
126338831 12633883 Fatigue
126338831 12633883 Gait disturbance
126338831 12633883 Hypertension
126338831 12633883 Ill-defined disorder
126338831 12633883 Mouth ulceration
126338831 12633883 Muscular weakness
126338831 12633883 Oral pain
126338831 12633883 Pain
126338831 12633883 Pyrexia
126338831 12633883 Rhinorrhoea
126338831 12633883 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