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
125230812 12523081 2 F 20160630 20160701 20160708 EXP PHHY2016TR089393 NOVARTIS EROL AM, CELIK C, YALBUZDAG SA, SENTURK B. STROKE FOLLOWING ZOLEDRONIC ACID INFUSION: EFFECT OF TREATMENT OR COINCIDENCE?. TURK J PHYS MED REHAB. 2016;62:170-3 67.00 YR M Y 0.00000 20160708 OT TR TR

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
125230812 12523081 1 PS ZOLEDRONIC ACID ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 5 MG, UNK U 0 5 MG
125230812 12523081 2 C CALCIUM CARBONATE. CALCIUM CARBONATE 1 Unknown 1200 MG, QD U 0 1200 MG QD
125230812 12523081 3 C VITAMIN D CHOLECALCIFEROL 1 Unknown 800 IU, QD U 0 800 IU QD
125230812 12523081 4 C CARBAMAZEPINE. CARBAMAZEPINE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125230812 12523081 1 Osteoporosis
125230812 12523081 2 Mineral supplementation
125230812 12523081 3 Vitamin supplementation
125230812 12523081 4 Seizure

Outcome of event

Event ID CASEID OUTC COD
125230812 12523081 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125230812 12523081 Blood calcium decreased
125230812 12523081 Cerebrovascular accident
125230812 12523081 Confusional state
125230812 12523081 Pyrexia
125230812 12523081 Somnolence
125230812 12523081 Urinary incontinence

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

no results found

Therapies reported

no results found