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
98681673 9868167 3 F 20160811 20140204 20160818 EXP PHHY2014BR011854 NOVARTIS 0.00 F Y 65.00000 KG 20160818 MD BR BR

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
98681673 9868167 1 PS ACLASTA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 5 MG, Q12MO 21817 5 MG SOLUTION FOR INJECTION
98681673 9868167 2 C FORASEQ BUDESONIDEFORMOTEROL FUMARATE 1 Unknown 1 DF (BUDESONIDE 12 UG, FORMOTEROL FUMARATE 400 UG), PRN 0 1 DF CAPSULE
98681673 9868167 3 C HYGROTON CHLORTHALIDONE 1 Unknown 50 MG, UNK 0 50 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
98681673 9868167 1 Osteoporosis
98681673 9868167 2 Bronchitis
98681673 9868167 3 Hypertension

Outcome of event

Event ID CASEID OUTC COD
98681673 9868167 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
98681673 9868167 Anaemia
98681673 9868167 Asthenia
98681673 9868167 Back pain
98681673 9868167 Concomitant disease aggravated
98681673 9868167 Herpes zoster
98681673 9868167 Immunodeficiency
98681673 9868167 Insomnia
98681673 9868167 Intervertebral disc protrusion
98681673 9868167 Malaise
98681673 9868167 Neuropathy peripheral
98681673 9868167 Obesity
98681673 9868167 Platelet disorder
98681673 9868167 Spinal disorder
98681673 9868167 Spinal pain
98681673 9868167 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
98681673 9868167 1 201312 0
98681673 9868167 2 2001 0
98681673 9868167 3 2004 0