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
123438893 12343889 3 F 201509 20160725 20160507 20160801 EXP PHEH2016US009924 SANDOZ 82.26 YR F Y 0.00000 20160801 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
123438893 12343889 1 SS LETROZOL LETROZOLE 1 Unknown 2.5 MG, QD (DAILY) U 0 2.5 MG QD
123438893 12343889 2 PS AMLODIPINE BESYLATE. AMLODIPINE BESYLATE 1 Unknown U 76859
123438893 12343889 3 SS CALCIUM CITRATE CALCIUM CITRATE 1 Unknown 300 MG, UNK Y 0 300 MG TABLET
123438893 12343889 4 SS CALCIUM CITRATE CALCIUM CITRATE 1 Unknown 250 MG, QD Y 0 250 MG TABLET QD
123438893 12343889 5 SS FOSAMAX ALENDRONATE SODIUM 1 Unknown UNK Y 0
123438893 12343889 6 SS ALENDRONATE ALENDRONATE SODIUM 1 Unknown 70 MG, QW EMPTY STOMACH U 0 70 MG /wk
123438893 12343889 7 C KLOR-CON POTASSIUM CHLORIDE 1 Unknown U 0
123438893 12343889 8 C VITAMIN D CHOLECALCIFEROL 1 Unknown UNK IU, UNK U 0
123438893 12343889 9 C CALCIUM CARBONATE. CALCIUM CARBONATE 1 Unknown U 0
123438893 12343889 10 C ZOMAX ZOMEPIRAC SODIUM 1 Unknown U 0
123438893 12343889 11 C CENTRUM SILVER ADULTS 50+ MINERALSVITAMINS 1 Unknown UNK UNK, QD U 0 QD
123438893 12343889 12 C ASPIRIN /00346701/ ASCORBIC ACIDASPIRIN 1 Unknown 87 MG, UNK U 0 87 MG
123438893 12343889 13 C TYLENOL ACETAMINOPHEN 1 Unknown UNK UNK, PRN U 0
123438893 12343889 14 C CALCIUM CALCIUM 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123438893 12343889 1 Breast cancer
123438893 12343889 2 Product used for unknown indication
123438893 12343889 3 Bone disorder
123438893 12343889 5 Bone density abnormal
123438893 12343889 6 Bone density decreased
123438893 12343889 7 Product used for unknown indication
123438893 12343889 8 Product used for unknown indication
123438893 12343889 9 Product used for unknown indication
123438893 12343889 10 Product used for unknown indication
123438893 12343889 11 Bone density decreased
123438893 12343889 12 Abdominal pain upper
123438893 12343889 13 Product used for unknown indication
123438893 12343889 14 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123438893 12343889 HO
123438893 12343889 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123438893 12343889 Arthralgia
123438893 12343889 Asthenia
123438893 12343889 Back pain
123438893 12343889 Balance disorder
123438893 12343889 Blister
123438893 12343889 Blood cholesterol increased
123438893 12343889 Dizziness
123438893 12343889 Dysphonia
123438893 12343889 Dysstasia
123438893 12343889 Eye swelling
123438893 12343889 Eyelid oedema
123438893 12343889 Fall
123438893 12343889 Gait disturbance
123438893 12343889 Hypersensitivity
123438893 12343889 Hypoacusis
123438893 12343889 Immune system disorder
123438893 12343889 Malaise
123438893 12343889 Osteoporosis
123438893 12343889 Pain
123438893 12343889 Pain in extremity
123438893 12343889 Rash
123438893 12343889 Sciatica
123438893 12343889 Somnolence
123438893 12343889 Spinal fracture
123438893 12343889 Swelling
123438893 12343889 Swelling face
123438893 12343889 Throat lesion
123438893 12343889 Vision blurred
123438893 12343889 Visual impairment
123438893 12343889 Weight 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
123438893 12343889 1 201509 0
123438893 12343889 3 201509 0
123438893 12343889 4 20150826 0
123438893 12343889 5 20160106 0
123438893 12343889 11 2005 0