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
100270286 10027028 6 F 20120827 20160822 20140321 20160830 EXP PHEH2014US005162 NOVARTIS 60.79 YR F Y 90.70000 KG 20160830 CN COUNTRY NOT SPECIFIED 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
100270286 10027028 1 PS GILENYA FINGOLIMOD HYDROCHLORIDE 1 Oral 0.5 MG, DAILY 161.145004 MG Y S0038 22527 .5 MG CAPSULE QD
100270286 10027028 2 C COREG CARVEDILOL 1 Unknown U 0
100270286 10027028 3 C CELEBREX CELECOXIB 1 Unknown U 0
100270286 10027028 4 C NORVASC AMLODIPINE BESYLATE 1 Unknown U 0
100270286 10027028 5 C FEMARA LETROZOLE 1 Unknown U 0
100270286 10027028 6 C TRIAMTERENE AND HYDROCHLOROTHIAZIDE HYDROCHLOROTHIAZIDETRIAMTERENE 1 Unknown 37.5/25 MG, DAILY U 0
100270286 10027028 7 C IBUPROFEN. IBUPROFEN 1 Unknown U 0
100270286 10027028 8 C LEXAPRO ESCITALOPRAM OXALATE 1 Unknown U 0
100270286 10027028 9 C MOBIC MELOXICAM 1 Unknown U 0
100270286 10027028 10 C LETROZOLE. LETROZOLE 1 Unknown 2.5 MG, DAILY U 0 2.5 MG
100270286 10027028 11 C AMLODIPINE AMLODIPINE BESYLATE 1 Unknown 10 MG, BID U 0 10 MG BID
100270286 10027028 12 C CARVEDILOL. CARVEDILOL 1 Unknown 25 MG, BID U 0 25 MG BID
100270286 10027028 13 C HEPARIN HEPARIN SODIUM 1 Subcutaneous 5000 U, Q12H U 0 5000 DF Q12H
100270286 10027028 14 C LIPITOR ATORVASTATIN CALCIUM 1 Unknown 20 MG, AT BEDTIME U 0 20 MG
100270286 10027028 15 C MIRALAX POLYETHYLENE GLYCOL 3350 1 Unknown 17 G, DAILY U 0 17 G
100270286 10027028 16 C BIDIL HYDRALAZINE HYDROCHLORIDEISOSORBIDE DINITRATE 1 Unknown U 0
100270286 10027028 17 C ELIQUIS APIXABAN 1 Unknown U 0
100270286 10027028 18 C LASIX FUROSEMIDE 1 Unknown U 0
100270286 10027028 19 C METOPROLOL TARTRATE. METOPROLOL TARTRATE 1 Unknown U 0
100270286 10027028 20 C POTASSIUM CHLORIDE. POTASSIUM CHLORIDE 1 Unknown U 0
100270286 10027028 21 C PROCARDIA NIFEDIPINE 1 Unknown U 0
100270286 10027028 22 C SPIRONOLACTONE. SPIRONOLACTONE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100270286 10027028 1 Multiple sclerosis
100270286 10027028 2 Product used for unknown indication
100270286 10027028 3 Product used for unknown indication
100270286 10027028 4 Product used for unknown indication
100270286 10027028 5 Product used for unknown indication
100270286 10027028 6 Product used for unknown indication
100270286 10027028 7 Product used for unknown indication
100270286 10027028 8 Product used for unknown indication
100270286 10027028 9 Product used for unknown indication
100270286 10027028 10 Product used for unknown indication
100270286 10027028 11 Product used for unknown indication
100270286 10027028 12 Product used for unknown indication
100270286 10027028 13 Product used for unknown indication
100270286 10027028 14 Product used for unknown indication
100270286 10027028 15 Constipation
100270286 10027028 16 Product used for unknown indication
100270286 10027028 17 Product used for unknown indication
100270286 10027028 18 Product used for unknown indication
100270286 10027028 19 Product used for unknown indication
100270286 10027028 20 Product used for unknown indication
100270286 10027028 21 Product used for unknown indication
100270286 10027028 22 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
100270286 10027028 DS
100270286 10027028 HO
100270286 10027028 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
100270286 10027028 Aortic valve incompetence
100270286 10027028 Balance disorder
100270286 10027028 Binocular eye movement disorder
100270286 10027028 Blood potassium decreased
100270286 10027028 Blood pressure decreased
100270286 10027028 Central nervous system lesion
100270286 10027028 Cerebrovascular accident
100270286 10027028 Decreased vibratory sense
100270286 10027028 Dizziness
100270286 10027028 Dysarthria
100270286 10027028 Dyskinesia
100270286 10027028 Facial pain
100270286 10027028 Gait disturbance
100270286 10027028 Gait spastic
100270286 10027028 Glucose tolerance impaired
100270286 10027028 Headache
100270286 10027028 Hemiparesis
100270286 10027028 High density lipoprotein decreased
100270286 10027028 Hypertension
100270286 10027028 Hypoaesthesia
100270286 10027028 Joint swelling
100270286 10027028 Knee deformity
100270286 10027028 Low density lipoprotein increased
100270286 10027028 Mitral valve incompetence
100270286 10027028 Muscular weakness
100270286 10027028 Musculoskeletal discomfort
100270286 10027028 Neck pain
100270286 10027028 Neurological symptom
100270286 10027028 Nuclear magnetic resonance imaging brain abnormal
100270286 10027028 Optic disc disorder
100270286 10027028 Osteoarthritis
100270286 10027028 Pain
100270286 10027028 Peripheral swelling
100270286 10027028 Pulmonary valve incompetence
100270286 10027028 Sleep apnoea syndrome
100270286 10027028 Speech disorder
100270286 10027028 Tricuspid valve incompetence
100270286 10027028 Type 2 diabetes mellitus
100270286 10027028 Urinary tract infection bacterial
100270286 10027028 Weight decreased
100270286 10027028 White blood cell count decreased

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
100270286 10027028 1 20111011 20141025 0