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This medication is indicated in post-menopausal women with osteoporosis (bone disorder in which bones become weak) to prevent fractures in them.
Patients using this medication may at times experience oesophageal ulcers, abdominal pain, and dyspepsia (indigestion). If you experience any of these symptoms for a long period of time, consult your doctor immediately.
This medication is not recommended in patients with kidney impairment (GFR<35 mL/min).
This medicine should not be taken with food
This medicine is used to treat the following:
Oral Form: Vitamin D deficiency due to decreased formation, malabsorption or liver disease, Hypocalcemia (decreased calcium levels) due to decreased parathyroid gland activity, or renal osteodystrophy (kidney) disease or disorder.
Injection Form: Vitamin D deficiency due to rickets (weak bones in children), osteomalacia (softening of bones), spasmophilia (impaired calcium utilization), Paget's disease (bone disease), osteoporomalacia (bone abnormality), and Fanconi syndrome (kidney disorder characterized by excretion of a substance in urine normally absorbed).
The patients administered with this medicine may experience anorexia, diarrhea, sweating, increased thirst, raised calcium and phosphate levels, and urinary changes.
The patients with severe disorders related to calcium disturbances, Vitamin-D disorders, parathyroid gland-related disorders, and renal (kidney) impairment should avoid the use of this medicine.
This medicine should be taken with food.
This medication should not be used in pregnancy.
The effects are undetermined; therefore, caution is advised. Consult your health care provider before use of this medicine.
This medication should not be used by lactating mothers.
The effects are undetermined; therefore, caution is advised. Consult your health care provider before use of this medicine.
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