Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Zoledronic acid
Drug ID BADD_D02392
Description Zoledronic acid, or CGP 42'446,[A203120] is a third generation, nitrogen containing bisphosphonate similar to [ibandronic acid], [minodronic acid], and [risedronic acid].[A203111] Zoledronic acid is used to treat and prevent multiple forms of osteoporosis, hypercalcemia of malignancy, multiple myeloma, bone metastases from solid tumors, and Paget’s disease of bone.[L13712,L13715,L13721] Zoledronic acid was first described in the literature in 1994.[A203120] Zoledronic acid was granted FDA approval on 20 August 2001.[L13712]
Indications and Usage For the treatment of hypercalcemia of malignancy. Also for the treatment of patients with multiple myeloma and patients with documented bone metastases from solid tumors, in conjunction with standard antineoplastic therapy. In May of 2007, the drug was approved for treatment of Paget’s Disease.
Marketing Status Prescription; Discontinued
ATC Code M05BA08
DrugBank ID DB00399
KEGG ID D01968
MeSH ID D000077211
PubChem ID 68740
TTD Drug ID D0VM2L
NDC Product Code 70860-802; 43598-255; 42533-102; 67457-794; 65797-0006; 65129-1144; 55111-688; 0078-0435; 67457-920; 50742-416; 55150-266; 54288-100; 55111-685; 0409-4215; 60505-6110; 16714-815; 68001-437; 55150-283; 25021-830; 65372-1117; 25021-826; 14593-836; 16729-242; 0143-9642; 57741-2600; 51991-065; 68001-366; 68083-142; 53104-7622; 25021-801; 43598-331; 17478-324; 70860-210; 63323-966; 68554-0037; 43598-330; 63126-906; 63759-0012; 62147-0125; 67457-619; 68083-116; 63850-7104; 68083-256; 17478-327; 68083-135; 63323-961; 67457-390
Synonyms Zoledronic Acid | 2-(Imidazol-1-yl)-1-hydroxyethylidene-1,1-bisphosphonic acid | CGP 42446A | CGP-42446 | CGP 42446 | CGP42446 | CGP-42'446 | CGP42'446 | CGP 42'446 | Zometa | Zoledronic Acid Anhydrous | Zoledronate
Chemical Information
Molecular Formula C5H10N2O7P2
CAS Registry Number 118072-93-8
SMILES C1=CN(C=N1)CC(O)(P(=O)(O)O)P(=O)(O)O
Chemical Structure
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Not AvailableNot AvailableNot AvailableNot AvailableNot Available
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Emphysema22.01.02.0020.005135%Not Available
Endocarditis11.01.16.001; 02.09.01.0010.003423%
Endophthalmitis11.01.06.003; 06.04.05.009--
Enteritis07.08.03.0020.019683%
Eosinophil count decreased13.01.06.0030.013122%Not Available
Episcleritis10.02.01.024; 06.04.07.001--Not Available
Epistaxis24.07.01.005; 22.04.03.001--
Erysipelas11.02.06.001; 23.09.01.0020.013122%Not Available
Erythema23.03.06.0010.544551%Not Available
Erythromelalgia24.03.01.001; 23.06.05.0020.013122%Not Available
Exophthalmos06.09.04.001; 05.02.02.0020.065609%Not Available
Exostosis15.02.04.0050.059048%
Extrasystoles02.03.02.0030.019683%Not Available
Extravasation08.01.03.0080.032804%Not Available
Eye disorder06.08.03.0010.078730%Not Available
Eye haemorrhage24.07.05.002; 06.07.02.0010.032804%Not Available
Eye inflammation06.04.05.0020.091852%Not Available
Eye irritation06.04.05.003--Not Available
Eye pain06.08.03.0020.255873%
Eye swelling06.08.03.0030.078730%Not Available
Eyelid oedema23.04.01.003; 10.01.05.001; 06.04.04.0040.039365%Not Available
Eyelid ptosis17.17.02.004; 06.05.01.0020.059048%Not Available
Face oedema23.04.01.004; 10.01.05.002; 08.01.07.003--
Facial pain08.01.08.0120.118095%
Facial paralysis17.04.03.008--Not Available
Failure to thrive19.07.05.001; 18.04.01.003; 14.03.02.0080.006846%Not Available
Fanconi syndrome03.06.01.001; 20.05.03.009; 14.01.01.0110.039365%Not Available
Fatigue08.01.01.002--
Fear19.06.03.0010.045926%Not Available
Feeling abnormal08.01.09.0140.268995%Not Available
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