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DRUGS & SUPPLEMENTS
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Duvadilan
When are you taking this medicine? |
Duvadilan uses
Duvadilan consists of Isoxsuprine Hydrochloride, Isoxsuprine Resinate.Isoxsuprine Hydrochloride:
- Description
- Indications
- Composition
- Dosageandadministration
- Contraindications and cautions
- Adverse reactions
- How supplied
Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA.
CAUTION: Federal Law prohibits dispensing without prescription
DESCRIPTION
Duvadilan (Isoxsuprine Hydrochloride) HCI occurs as a white odorless, crystalline powder, having a bitter
taste, It has a following structural formula
INDICATIONS
Based on a review of this drug by the National Academy of Sciences -National Research Council and / or other information, the FDA has classified the medications as follows :
Possibly Effective :
1. For the relief of symptoms associated with cerebral vascular insufficiency
2. In Peripheral vascular disease of arteriosclerosis obliterans, thromboangitis obliterans (Buerger's Disease) and Raynaud's disease.
Final classification of the less-than-effective indications requires further investigation.
COMPOSITION
Each tablet contains lsoxsuprine HCI 20 mg.
These tablets contain the following inactive ingredients: dibasic calcium phosphate (anhydrous), lactose, magnesium stearate. microcrystalline cellulose, povidone k30, and sodium starch glycolate.
DOSAGEANDADMINISTRATION
Oral:10 to 20 mg three or four times daily
CONTRAINDICATIONS AND CAUTIONS
Oral
There are no known contraindications to oral use when administered in recommended doses. Should not be given immediately postpartum or in the presence of arterial bleeding.
ADVERSE REACTIONS
On rare occasion, oral administration of the drug has been associated in time with the occurrences of hypotension, tachycardia, chest pain, nausea, vomiting, dizziness, abdominal distress, and severe rash. If rash appears, the drug should be discontinued.
Although available evidence suggests a temporal association of these reactions with Duvadilan (Isoxsuprine Hydrochloride), a casual relationship can be neither confirmed nor refuted.
β-Adrenergic receptor stimulants such as Duvadilan (Isoxsuprine Hydrochloride) hydrochloride have been used to inhibit pre-term labor. Maternal and fetal tachycardia may occur under such use. Hypocalcemia, hypoglycemia, hypotension and ileus have been reported to occur in infants whose mothers received Duvadilan (Isoxsuprine Hydrochloride). Pulmonary edema has been reported in mothers treated with β-stimulants. Duvadilan (Isoxsuprine Hydrochloride) HCl tablets, USP is neither approved nor recommended for use in the treatment of premature labor.
HOW SUPPLIED
Duvadilan (Isoxsuprine Hydrochloride) HCI tablets, USP are supplied in HDPE bottles.
20 mg Bottles of 1,000's: NDC61971-065-10
Manufactured in India by
Vista Pharmaceuticals, Limited.
For
Vista Pharmaceuticals, Inc.
Revised:07/2017
Isoxsuprine Resinate:
- Description
- Indications
- Composition
- Dosageandadministration
- Contraindications and cautions
- Adverse reactions
- How supplied
Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA.
CAUTION: Federal Law prohibits dispensing without prescription
DESCRIPTION
Duvadilan (Isoxsuprine Resinate) HCI occurs as a white odorless, crystalline powder, having a bitter
taste, It has a following structural formula
INDICATIONS
Based on a review of this drug by the National Academy of Sciences -National Research Council and / or other information, the FDA has classified the medications as follows :
Possibly Effective :
1. For the relief of symptoms associated with cerebral vascular insufficiency
2. In Peripheral vascular disease of arteriosclerosis obliterans, thromboangitis obliterans (Buerger's Disease) and Raynaud's disease.
Final classification of the less-than-effective indications requires further investigation.
COMPOSITION
Each tablet contains lsoxsuprine HCI 20 mg.
These tablets contain the following inactive ingredients: dibasic calcium phosphate (anhydrous), lactose, magnesium stearate. microcrystalline cellulose, povidone k30, and sodium starch glycolate.
DOSAGEANDADMINISTRATION
Oral:10 to 20 mg three or four times daily
CONTRAINDICATIONS AND CAUTIONS
Oral
There are no known contraindications to oral use when administered in recommended doses. Should not be given immediately postpartum or in the presence of arterial bleeding.
ADVERSE REACTIONS
On rare occasion, oral administration of the drug has been associated in time with the occurrences of hypotension, tachycardia, chest pain, nausea, vomiting, dizziness, abdominal distress, and severe rash. If rash appears, the drug should be discontinued.
Although available evidence suggests a temporal association of these reactions with Duvadilan (Isoxsuprine Resinate), a casual relationship can be neither confirmed nor refuted.
β-Adrenergic receptor stimulants such as Duvadilan (Isoxsuprine Resinate) hydrochloride have been used to inhibit pre-term labor. Maternal and fetal tachycardia may occur under such use. Hypocalcemia, hypoglycemia, hypotension and ileus have been reported to occur in infants whose mothers received Duvadilan (Isoxsuprine Resinate). Pulmonary edema has been reported in mothers treated with β-stimulants. Duvadilan (Isoxsuprine Resinate) HCl tablets, USP is neither approved nor recommended for use in the treatment of premature labor.
HOW SUPPLIED
Duvadilan (Isoxsuprine Resinate) HCI tablets, USP are supplied in HDPE bottles.
20 mg Bottles of 1,000's: NDC61971-065-10
Manufactured in India by
Vista Pharmaceuticals, Limited.
For
Vista Pharmaceuticals, Inc.
Revised:07/2017
Duvadilan pharmaceutical active ingredients containing related brand and generic drugs:
Duvadilan available forms, composition, doses:
Composition is the list of ingredients which combinedly form a medicine. Both active ingredients and inactive ingredients form the composition. The active ingredient gives the desired therapeutic effect whereas the inactive ingredient helps in making the medicine stable.
Doses are various strengths of the medicine like 10mg, 20mg, 30mg and so on. Each medicine comes in various doses which is decided by the manufacturer, that is, pharmaceutical company. The dose is decided on the severity of the symptom or disease.