DRUGS & SUPPLEMENTS
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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
Myprox HCI occurs as a white odorless, crystalline powder, having a bitter
taste, It has a following structural formula
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.
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.
Oral:10 to 20 mg three or four times daily
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.
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 Myprox, a casual relationship can be neither confirmed nor refuted.
β-Adrenergic receptor stimulants such as Myprox 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 Myprox. Pulmonary edema has been reported in mothers treated with β-stimulants. Myprox HCl tablets, USP is neither approved nor recommended for use in the treatment of premature labor.
Myprox 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.
Vista Pharmaceuticals, Inc.
Depending on the reaction of the Myprox after taken, if you are feeling dizziness, drowsiness or any weakness as a reaction on your body, Then consider Myprox not safe to drive or operate heavy machine after consumption. Meaning that, do not drive or operate heavy duty machines after taking the capsule if the capsule has a strange reaction on your body like dizziness, drowsiness. As prescribed by a pharmacist, it is dangerous to take alcohol while taking medicines as it exposed patients to drowsiness and health risk. Please take note of such effect most especially when taking Primosa capsule. It's advisable to consult your doctor on time for a proper recommendation and medical consultations.Is Myprox addictive or habit forming?
Medicines are not designed with the mind of creating an addiction or abuse on the health of the users. Addictive Medicine is categorically called Controlled substances by the government. For instance, Schedule H or X in India and schedule II-V in the US are controlled substances.
Please consult the medicine instruction manual on how to use and ensure it is not a controlled substance.In conclusion, self medication is a killer to your health. Consult your doctor for a proper prescription, recommendation, and guidiance.
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The information was verified by Dr. Rachana Salvi, MD Pharmacology