The Safety Rates Drug Report

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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
127419951 12741995 1 I 20160907 20160914 20160914 EXP PHEH2016US022720 NOVARTIS 0.00 F Y 0.00000 20160914 MD US US

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
127419951 12741995 1 PS GLEEVEC IMATINIB MESYLATE 1 Unknown 400 MG, UNK 21588 400 MG
127419951 12741995 2 SS GLEEVEC IMATINIB MESYLATE 1 Unknown 600 MG, UNK 21588 600 MG
127419951 12741995 3 C AMLODIPINE AMLODIPINE BESYLATE 1 Unknown UNK U 0
127419951 12741995 4 C METOPROLOL TARTRATE. METOPROLOL TARTRATE 1 Unknown UNK U 0
127419951 12741995 5 C CALCIUM + VIT D CALCIUMVITAMIN D 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127419951 12741995 1 Product used for unknown indication
127419951 12741995 3 Product used for unknown indication
127419951 12741995 4 Product used for unknown indication
127419951 12741995 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127419951 12741995 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127419951 12741995 Alopecia
127419951 12741995 Asthenia
127419951 12741995 Bone pain
127419951 12741995 Immunodeficiency
127419951 12741995 Nausea
127419951 12741995 Neoplasm recurrence
127419951 12741995 Ocular hyperaemia
127419951 12741995 Pain in extremity
127419951 12741995 Peripheral swelling
127419951 12741995 Skin discolouration
127419951 12741995 Sleep disorder
127419951 12741995 Vision blurred
127419951 12741995 Vomiting
127419951 12741995 Weight decreased

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

no results found

Therapies reported

no results found