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
125412181 12541218 1 I 20160705 20160708 20160708 EXP PHHY2016CA093631 NOVARTIS 58.00 YR F Y 77.00000 KG 20160708 OT CA CA

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
125412181 12541218 1 PS ACLASTA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 100 ML, ONCE/SINGLE 21817 100 ML SOLUTION FOR INJECTION 1X
125412181 12541218 2 C ARIMIDEX ANASTROZOLE 1 Unknown UNK U 0 TABLET
125412181 12541218 3 C NAPROXEN. NAPROXEN 1 Unknown UNK U 0
125412181 12541218 4 C NASONEX MOMETASONE FUROATE 1 Unknown UNK U 0 SPRAY

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125412181 12541218 1 Osteoporosis
125412181 12541218 2 Product used for unknown indication
125412181 12541218 3 Product used for unknown indication
125412181 12541218 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125412181 12541218 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125412181 12541218 Arthralgia
125412181 12541218 Asthenia
125412181 12541218 Fatigue
125412181 12541218 Headache
125412181 12541218 Lethargy
125412181 12541218 Lymphadenopathy
125412181 12541218 Musculoskeletal stiffness
125412181 12541218 Myalgia
125412181 12541218 Nausea
125412181 12541218 Oropharyngeal pain

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

no results found

Therapies reported

no results found