More Information About - Bondrova 150 mg Tab. - 150mg
Description
Generic Name
Ibandronic Acid
Precaution
History of bone/joint/muscle pain; dysphagia, oesophageal disease, gastritis, duodenitis, ulcers. Risk factors for osteonecrosis of the jaw. Pregnancy and lactation.
Indication
Post-menopausal osteoporosis, Hypercalcaemia of malignancy, Breast cancer, bone metastases
Contra Indication
Severe renal impairment, uncorrected hypocalcaemia, acute upper GI inflammation, inability to stand or sit upright for at least 60 min (oral).
Dose
N/A
Side Effect
Flu-like symptoms (e.g. myalgia, arthralgia, fever, chills, fatigue, nausea, loss of appetite, bone pain), atypical fractures, osteonecrosis of the jaw, ocular inflammation, acute renal failure, hypocalcaemia, musculoskeletal pain. Rarely, anaemia, bronchospasm, taste disturbance, paraesthesia, uraemia; transient fever (IV); abdominal pain, dyspepsia, severe oesophageal reactions (oral).)
Potentially Fatal: Anaphylactic reaction/shock.
Pregnancy Category
Name :
C
Description
Animal reproduction studies have shown an adverse effect on the fetus and there are no adequate and well-controlled studies in humans, but potential benefits may warrant use of the drug in pregnant women despite potential risks
Mode of Action
Ibandronic acid is a potent bone resorption inhibitor, which acts on osteoclasts or on osteoclast precursors. It increases bone mineral density by reducing the rate of bone resorption.
Interaction
Decreased absorption w/ Ca supplements, antacids and other multivalent cation-containing oral drugs. Increased incidence of GI irritation w/ aspirin or NSAIDs.
Pregnancy Category Note
N/A
Adult Dose
Oral
Prophylaxis of skeletal events in patients with breast cancer and bone metastases
Adult: 50 mg daily.
Postmenopausal osteoporosis; Prophylaxis of postmenopausal osteoporosis
Adult: 150 mg once mthly on the same date each mth, alternatively, 2.5 mg daily. Missed once-mthly dose: If next scheduled dose is >7 days away: Take dose the next morning and return to original schedule; if next dose is <7 days away: Wait until the next scheduled dose; 2 tabs must not be taken w/in the same wk.
Intravenous
Hypercalcaemia of malignancy
Adult: 2-4 mg as a single infusion over 2 hr. Max: 6 mg.
Postmenopausal osteoporosis
Adult: 3 mg by inj over 15-30 seconds once every 3 mth. Missed dose: Give inj as soon as possible; then re-schedule next inj 3 mth from this inj; should not be given more frequently than once every 3 mth.
Prophylaxis of skeletal events in patients with breast cancer and bone metastases
Adult: 6 mg by infusion over at least 15 min 3-4 wkly.
Child Dose
N/A
Renal Dose
Oral
Prophylaxis of skeletal events in patients with breast cancer and bone metastases
Renal impairment:
CrCl (ml/min) Dosage Recommendation
<30 50 mg once wkly.
30-49 50 mg every other day.
Oral: Postmenopausal osteoporosis; Prophylaxis of postmenopausal osteoporosis
Intravenous: Hypercalcaemia of malignancy, Postmenopausal osteoporosis
Renal impairment:
CrCl (ml/min) Dosage Recommendation
<30 Not recommended.
Intravenous
Prophylaxis of skeletal events in patients with breast cancer and bone metastases
Renal impairment:
CrCl (ml/min) Dosage Recommendation
<30 2 mg in 500 mL soln infused over 1 hr 3-4 wkly.
30-49 4 mg in 500 mL soln infused over 1 hr 3-4 wkly.
Administration
Should be taken on an empty stomach. Must be taken at least 1 hr before the 1st food, drink or medication of the day. Take w/ a full glass of only plain water upon arising for the day & remain in sitting/upright position for at least 1 hr. Do not lie down, eat/drink anything except plain water or take other oral medicines for at least 1 hr. Swallow whole, do not chew/crush/suck.
Reconstitution: Add contents of vial to 100-500 mL of NaCl 0.9% or dextrose 5%.
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The information provided herein are for informational purposes only and not intended to be a substitute for professional medical advice, diagnosis, or treatment. Please note that this information should not be treated as a replacement for physical medical consultation or advice. Great effort has been placed to provide accurate and comprehensive data. However, Medicart along with its authors and editors make no representations or warranties and specifically disclaim all liability for any medical information provided on the site. The absence of any information and/or warning to any drug shall not be considered and assumed as an implied assurance of the Company.