Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Alendronic acid
Drug ID BADD_D00066
Description Alendronic acid is a second generation bisphosphonate that is used for the treatment of some forms of osteoperosis and Paget's disease[FDA Label][A959,A203111]. It functions by preventing resorption of bone[FDA Label][A959].
Indications and Usage Alendronic acid is indicated for the treatment and prevention of osteoporosis in men and postmenopausal women, treatment of glucocorticoid-induced osteoporosis, and Paget's disease of bone[FDA Label][A959,A176750]. However, alendronic acid is not indicated for use in pediatric populations or patients with a creatinine clearance <35mL/min[FDA Label].
Marketing Status approved
ATC Code M05BA04
DrugBank ID DB00630
KEGG ID D07119
MeSH ID D019386
PubChem ID 2088
TTD Drug ID D09KLR
NDC Product Code Not Available
UNII X1J18R4W8P
Synonyms Alendronate | 4-Amino-1-Hydroxybutylidene 1,1-Biphosphonate | Aminohydroxybutane Bisphosphonate | MK-217 | MK 217 | MK217 | Alendronate Monosodium Salt, Trihydrate | Alendronate Sodium | Fosamax
Chemical Information
Molecular Formula C4H13NO7P2
CAS Registry Number 66376-36-1
SMILES C(CC(O)(P(=O)(O)O)P(=O)(O)O)CN
Chemical Structure
ADRs Induced by Drug
*The priority for ADR severity classification is based on FAERS assessment, followed by the most severe level in CTCAE rating. If neither is available, it will be displayed as 'Not available'.
**The 'Not Available' level is hidden by default and can be restored by clicking on the legend twice..
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Vitamin D deficiency14.12.03.0030.003456%Not Available
Vitiligo23.05.02.004; 10.04.02.0040.000088%Not Available
Vitreous detachment12.01.04.005; 06.09.01.0020.000110%Not Available
Vitreous floaters06.09.01.0050.000088%
Vomiting07.01.07.003--
Vulval ulceration23.07.03.013; 21.08.01.0130.000088%Not Available
Vulvovaginal discomfort21.08.02.0050.000044%Not Available
Vulvovaginal dryness21.08.02.0030.000132%
Wheezing22.03.01.0090.000308%
Mental status changes19.07.01.0010.000264%Not Available
Tubulointerstitial nephritis20.05.02.0020.000066%Not Available
Mobility decreased15.03.05.023; 17.02.05.018; 08.01.03.0300.000176%Not Available
Fibromyalgia15.05.02.0020.000594%Not Available
Musculoskeletal disorder15.03.05.0250.000361%Not Available
Intestinal polyp16.05.01.002; 07.20.01.0090.000088%Not Available
Joint range of motion decreased15.01.02.0060.000066%
Myofascial pain syndrome15.05.02.0030.000242%Not Available
Breast calcifications21.05.04.0090.000132%Not Available
Deafness unilateral04.02.01.0110.000044%Not Available
Underweight14.03.02.0170.000044%Not Available
Ischaemic cardiomyopathy24.04.04.019; 02.04.01.0040.000110%Not Available
Hypoacusis04.02.01.0060.000528%
Onychoclasis23.02.05.0050.000119%Not Available
Seasonal allergy22.04.04.008; 10.01.04.001; 06.04.01.0130.000462%Not Available
Paradoxical drug reaction08.06.01.0140.000132%Not Available
Carotid artery occlusion24.04.06.008; 17.08.01.0120.000066%Not Available
Bladder spasm20.02.02.0130.000044%
Acute phase reaction08.01.05.004--Not Available
Scar pain23.03.03.0600.000044%Not Available
Weight fluctuation14.03.02.0020.000088%Not Available
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