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
101721303 10172130 3 F 2013 20160726 20140515 20160803 EXP DK-DKMA-ADR 22411968 PHHY2014DK057093 NOVARTIS 53.38 YR F Y 72.00000 KG 20160803 OT DK DK

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
101721303 10172130 1 PS ACLASTA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 5 MG/ML, UNK 5 MG 21817 SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
101721303 10172130 1 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
101721303 10172130 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
101721303 10172130 Arthralgia
101721303 10172130 Asthenia
101721303 10172130 Bone pain
101721303 10172130 Constipation
101721303 10172130 Diarrhoea
101721303 10172130 Dizziness
101721303 10172130 Dyspnoea
101721303 10172130 Eye pain
101721303 10172130 Fatigue
101721303 10172130 Fibromyalgia
101721303 10172130 Gait disturbance
101721303 10172130 Gastrointestinal motility disorder
101721303 10172130 Gout
101721303 10172130 Headache
101721303 10172130 Hypoaesthesia
101721303 10172130 Impaired healing
101721303 10172130 Muscle spasms
101721303 10172130 Musculoskeletal stiffness
101721303 10172130 Pain in extremity
101721303 10172130 Pelvic pain
101721303 10172130 Peripheral swelling
101721303 10172130 Rash
101721303 10172130 Thirst

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
101721303 10172130 1 20130923 20130923 0