Vaccinosis Nosode
Generic Name: vaccinosis nosode
Brand Names:
Vaccinosis Nosode 4004
*Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Overview
*Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Uses
INDICATIONS For the temporary relief of aches, pains, or stiffness of muscles or joints, occasional headache, tiredness, or upset stomach.*
Dosage
DIRECTIONS Place drops under tongue 30 minutes before/after meals. Adults and children 12 years and over: Take 10 to 15 drops once weekly or monthly. If mild symptoms are present, take 10 drops up to 3 times per day. Consult a physician for use in children under 12 years of age.
Warnings
WARNINGS Consult a doctor if condition worsens or if symptoms persist. Keep out of the reach of children. In case of overdose, get medical help or contact a poison control center right away. If pregnant or breastfeeding, ask a healthcare professional before use. Keep out of the reach of children. If pregnant or breastfeeding, ask a healthcare professional before use.
Pregnancy
If pregnant or breastfeeding, ask a healthcare professional before use.
Frequently Asked Questions
What is Vaccinosis Nosode used for?▼
INDICATIONS For the temporary relief of aches, pains, or stiffness of muscles or joints, occasional headache, tiredness, or upset stomach.*
Can I take Vaccinosis Nosode during pregnancy?▼
If pregnant or breastfeeding, ask a healthcare professional before use.
What are the important warnings for Vaccinosis Nosode?▼
WARNINGS Consult a doctor if condition worsens or if symptoms persist. Keep out of the reach of children. In case of overdose, get medical help or contact a poison control center right away. If pregnant or breastfeeding, ask a healthcare professional before use. Keep out of the reach of children. If pregnant or breastfeeding, ask a healthcare professional before use.
Related Medications
Allium Sativum, Avena Sativa, Berberis Vulgaris, Lappa Major, Solidago Virgaurea, Phytolacca Decandra, Lycopodium Clavatum, Nux Vomica, Aluminium Metallicum, Antimonium Crudum, Argentum Metallicum, Arsenicum Album, Aurum Metallicum, Baryta Carbonica, Beryllium Metallicum, Bismuthum Metallicum, Boron, Bromium, Cadmium Metallicum, Cerium Metallicum, Cesium Chloride, Chromium, Cobaltum Metallicum, Cuprum Metallicum, Dysprosium Metallicum, Erbium Metallicum, Europium Metallicum, Ferrum Metallicum, Molybdenum,
allium sativum, avena sativa, berberis vulgaris, lappa major, solidago virgaurea, phytolacca decandra, lycopodium clavatum, nux vomica, aluminium metallicum, antimonium crudum, argentum metallicum, arsenicum album, aurum metallicum, baryta carbonica, beryllium metallicum, bismuthum metallicum, boron, bromium, cadmium metallicum, cerium metallicum, cesium chloride, chromium, cobaltum metallicum, cuprum metallicum, dysprosium metallicum, erbium metallicum, europium metallicum, ferrum metallicum, molybdenum,
Standardized Chemical Allergen [EPC]
INDICATIONS: May temporarily relieve vomiting, exhaustion, and metallic taste.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Ulex Europaeus Whole
ulex europaeus whole
Hopelessness, despair.
Epoprostenol
epoprostenol
Prostacycline Vasodilator [EPC]
11 DESCRIPTION Epoprostenol sodium is the sodium salt of epoprostenol, formulated as a white to off-white lyophilized cake or powder for intravenous (IV) administration. Each vial of Epoprostenol for Injection contains epoprostenol sodium equivalent to either 0.5 mg (500,000 ng) or 1.5 mg (1,500,000 ng) epoprostenol, 5 mg Glycine and 100 mg sucrose. Sodium hydroxide is added to adjust pH.
Medical Disclaimer
This drug information is for educational purposes only and should not replace professional medical advice. Drug information is sourced from the FDA National Drug Code Directory and Structured Product Labeling. Always consult with a healthcare provider before starting, stopping, or changing any medication.