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
125840211 12584021 1 I 20160712 20160722 20160722 EXP PT-MYLANLABS-2016M1029522 MYLAN RUI VALENTE ET AL,. POLINEUROPATIA SENSITIVO-MOTOVA-UM CASO DE TOXICIDADE A AMIODARONA. CONGRESSO NACIONAL DE MEDICINA INTERNA. 113 0.00 Y 0.00000 20160722 MD PT PT

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
125840211 12584021 1 PS AMIODARONE AMIODARONE 1 Unknown UNK U U 76217
125840211 12584021 2 SS ENALAPRIL ENALAPRIL 1 Unknown UNK U U 0
125840211 12584021 3 SS TAMSULOSIN TAMSULOSIN 1 UNK U U 0
125840211 12584021 4 SS SPIRONOLACTONE. SPIRONOLACTONE 1 Unknown UNK U U 0
125840211 12584021 5 SS FUROSEMIDE. FUROSEMIDE 1 Unknown UNK U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125840211 12584021 1 Product used for unknown indication
125840211 12584021 2 Product used for unknown indication
125840211 12584021 3 Product used for unknown indication
125840211 12584021 4 Product used for unknown indication
125840211 12584021 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125840211 12584021 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125840211 12584021 Acute kidney injury
125840211 12584021 Asthenia
125840211 12584021 Condition aggravated
125840211 12584021 Fall
125840211 12584021 Gait disturbance
125840211 12584021 Hypoaesthesia
125840211 12584021 Mediastinal disorder
125840211 12584021 Peripheral sensorimotor neuropathy
125840211 12584021 Resting tremor

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

no results found

Therapies reported

no results found