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
124592733 12459273 3 F 2012 20160809 20160613 20160822 EXP PHEH2016US013560 NOVARTIS 82.00 YR F Y 0.00000 20160822 CN 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
124592733 12459273 1 PS LETROZOLE. LETROZOLE 1 Unknown 1 DF (1 DAILY) U 20726 1 DF
124592733 12459273 2 SS CALCIUM CITRATE CALCIUM CITRATE 1 Unknown 250 MG, UNK U 0 250 MG TABLET
124592733 12459273 3 SS PERCOCET ACETAMINOPHENOXYCODONE HYDROCHLORIDE 1 Unknown U 0
124592733 12459273 4 C AMLODIPINE AMLODIPINE BESYLATE 1 Unknown 15 MG (15 MG OR 10 MG) U 0 15 MG TABLET
124592733 12459273 5 C POTASSIUM POTASSIUM 1 Unknown 1 DF, (1 TABLET) U 0 1 DF TABLET
124592733 12459273 6 C PREVALITE CHOLESTYRAMINE 1 Unknown U 0 POWDER
124592733 12459273 7 C DRAMAMINE DIMENHYDRINATE 1 Unknown AS NEEDED U 0
124592733 12459273 8 C TYLENOL ACETAMINOPHEN 1 Unknown AS NEEDED U 0
124592733 12459273 9 C CENTRUM SILVER MINERALSVITAMINS 1 Unknown 1 DF, QD (1 TABLET DAILY) U 0 1 DF TABLET QD
124592733 12459273 10 C FOSAMAX ALENDRONATE SODIUM 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124592733 12459273 1 Breast cancer
124592733 12459273 2 Product used for unknown indication
124592733 12459273 3 Product used for unknown indication
124592733 12459273 4 Product used for unknown indication
124592733 12459273 5 Product used for unknown indication
124592733 12459273 6 Product used for unknown indication
124592733 12459273 7 Product used for unknown indication
124592733 12459273 8 Product used for unknown indication
124592733 12459273 9 Product used for unknown indication
124592733 12459273 10 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124592733 12459273 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124592733 12459273 Aortic valve incompetence
124592733 12459273 Arthralgia
124592733 12459273 Balance disorder
124592733 12459273 Blood cholesterol increased
124592733 12459273 Calcium metabolism disorder
124592733 12459273 Dizziness
124592733 12459273 Dysphonia
124592733 12459273 Eye swelling
124592733 12459273 Eyelid oedema
124592733 12459273 Fall
124592733 12459273 Foot fracture
124592733 12459273 Gait disturbance
124592733 12459273 Hearing disability
124592733 12459273 Initial insomnia
124592733 12459273 Oedema peripheral
124592733 12459273 Osteoporosis
124592733 12459273 Paraesthesia
124592733 12459273 Rash
124592733 12459273 Sciatica
124592733 12459273 Spinal fracture
124592733 12459273 Swelling face
124592733 12459273 Vomiting

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

no results found

Therapies reported

no results found