NALTREXONE HYDROCHLORIDE tablet, film coated USA - engelsk - NLM (National Library of Medicine)

naltrexone hydrochloride tablet, film coated

a-s medication solutions - naltrexone hydrochloride (unii: z6375yw9sf) (naltrexone - unii:5s6w795cqm) - naltrexone hydrochloride tablets usp are indicated in the treatment of alcohol dependence and for the blockade of the effects of exogenously administered opioids. naltrexone hydrochloride tablets usp have not been shown to provide any therapeutic benefit except as part of an appropriate plan of management for the addictions. naltrexone hydrochloride is contraindicated in: - patients receiving opioid analgesics. - patients currently dependent on opioids, including those currently maintained on opiate agonists (e.g., methadone) or partial agonists (e.g., buprenorphine). - patients in acute opioid withdrawal (see warnings ). - any individual who has failed the naloxone challenge test or who has a positive urine screen for opioids. - any individual with a history of sensitivity to naltrexone hydrochloride or any other components of this product. it is not known if there is any cross-sensitivity with naloxone or the phenanthrene containing opioids. naltrexone hydrochloride is a pure opioid antagonist. it does not

NALTREXONE HYDROCHLORIDE tablet, film coated USA - engelsk - NLM (National Library of Medicine)

naltrexone hydrochloride tablet, film coated

a-s medication solutions - naltrexone hydrochloride (unii: z6375yw9sf) (naltrexone - unii:5s6w795cqm) - naltrexone hydrochloride tablets are indicated in the treatment of alcohol dependence and for the blockade of the effects of exogenously administered opioids. naltrexone hydrochloride has not been shown to provide any therapeutic benefit except as part of an appropriate plan of management for the addictions. naltrexone hydrochloride is contraindicated in: - patients receiving opioid analgesics. - patients currently dependent on opioids, including those currently maintained on opiate agonists [e.g., methadone) or partial agonists (e.g., buprenorphine). - patients in acute opioid withdrawal (see warnings). - any individual who has failed the naloxone challenge test or who has a positive urine screen for opioids. - any individual with a history of sensitivity to naltrexone hydrochloride or any other components of this product. it is not known if there is any cross-sensitivity with naloxone or the phenanthrene containing opioids. naltrexone hydrochloride is a pure opioid antagonist. it does not lead to physical o

NALTREXONE HYDROCHLORIDE tablet, film coated USA - engelsk - NLM (National Library of Medicine)

naltrexone hydrochloride tablet, film coated

a-s medication solutions - naltrexone hydrochloride (unii: z6375yw9sf) (naltrexone - unii:5s6w795cqm) - naltrexone hydrochloride tablets usp are indicated in the treatment of alcohol dependence and for the blockade of the effects of exogenously administered opioids. naltrexone hydrochloride tablets usp have not been shown to provide any therapeutic benefit except as part of an appropriate plan of management for the addictions. naltrexone hydrochloride is contraindicated in: - patients receiving opioid analgesics. - patients currently dependent on opioids, including those currently maintained on opiate agonists (e.g., methadone) or partial agonists (e.g., buprenorphine). - patients in acute opioid withdrawal (see warnings ). - any individual who has failed the naloxone challenge test or who has a positive urine screen for opioids. - any individual with a history of sensitivity to naltrexone hydrochloride or any other components of this product. it is not known if there is any cross-sensitivity with naloxone or the phenanthrene containing opioids. naltrexone hydrochloride is a pure opioid antagonist. it does not

VIATREXX-MUSKELNEURAL- anti-interleukin-1.alpha. injection USA - engelsk - NLM (National Library of Medicine)

viatrexx-muskelneural- anti-interleukin-1.alpha. injection

viatrexx bio incorporated - anti-interleukin-1.alpha. immunoglobulin g rabbit (unii: ml4qrz1hcl) (anti-interleukin-1.alpha. immunoglobulin g rabbit - unii:ml4qrz1hcl), bos taurus ankle joint (unii: 63z8otg0hu) (bos taurus ankle joint - unii:63z8otg0hu), sus scrofa ankle joint (unii: 654134quov) (sus scrofa ankle joint - unii:654134quov), bos taurus joint capsule (unii: 782i3o9vsm) (bos taurus joint capsule - unii:782i3o9vsm), sus scrofa joint capsule (unii: lx0xhe5nln) (sus scrofa joint capsule - unii:lx0xhe5nln), brain-derived neurot - viatrexx-muskelneural  a sterile, injectable, biodegradable, clear isotonic liquid that is injected into the various layers of the skin, muscles, ligaments, joints, other body tissues or added to an iv, either as a push or into the bag. this product should not be used in patients with a known hypersensitivity to any ingredient found in the formula, porcine products, isotonic saline or benzyl alcohol, or patients with a history of severe allergies. as with all injections, epinephrine injection (1:1,000) must be immediately available should an acute anaphylactoid reaction occur due to any component of the injection. this product contains 1% benzyl alcohol. benzyl alcohol has been reported to be associated with a fatal "gasping syndrome" in premature infants. due to the benzyl alcohol content, this product should not be given to a pregnant woman. this product should not be used in patients with a known hypersensitivity to any ingredient in this formula, porcine products, isotonic saline or benzyl alcohol, or pat

VIATREXX-IMMUNEXX- adrenal gland, ascorbic acid, bone marrow, erythrocytes, granulocyte colony-stimulating factor, interleukin 2 USA - engelsk - NLM (National Library of Medicine)

viatrexx-immunexx- adrenal gland, ascorbic acid, bone marrow, erythrocytes, granulocyte colony-stimulating factor, interleukin 2

viatrexx bio incorporated - bos taurus adrenal gland (unii: m2776swb29) (bos taurus adrenal gland - unii:m2776swb29), sus scrofa adrenal gland (unii: 398iyq16yv) (sus scrofa adrenal gland - unii:398iyq16yv), ascorbic acid (unii: pq6ck8pd0r) (ascorbic acid - unii:pq6ck8pd0r), bos taurus bone marrow (unii: 08x0k2m57p) (bos taurus bone marrow - unii:08x0k2m57p), sus scrofa bone marrow (unii: vp2cn2g7y8) (sus scrofa bone marrow - unii:vp2cn2g7y8), bos taurus red blood cell (unii: 5w4flb0u2c) (bos taurus red blood cell - unii:5w4flb0u2c), - viatrexx-immunexx  a sterile, injectable, biodegradable, clear isotonic liquid that is injected into the various layers of the skin, muscles, ligaments, joints, other body tissues or added to an iv, either as a push or into the bag. this product should not be used in patients with a known hypersensitivity to any ingredient found in the formula, porcine products, isotonic saline or benzyl alcohol, or patients with a history of severe allergies. as with all injections, epinephrine injection (1:1,000) must be immediately available should an acute anaphylactoid reaction occur due to any component of the injection. this product contains 1% benzyl alcohol. benzyl alcohol has been reported to be associated with a fatal "gasping syndrome" in premature infants. due to the benzyl alcohol content, this product should not be given to a pregnant woman. this product should not be used in patients with a known hypersensitivity to any ingredient in this formula, porcine products, isotonic saline or benzyl alcohol, or patient

VIATREXX-ITHURTS- anti-interleukin-1.alpha. apomorphine, metenkefalin injection USA - engelsk - NLM (National Library of Medicine)

viatrexx-ithurts- anti-interleukin-1.alpha. apomorphine, metenkefalin injection

viatrexx bio incorporated - anti-interleukin-1.alpha. immunoglobulin g rabbit (unii: ml4qrz1hcl) (anti-interleukin-1.alpha. immunoglobulin g rabbit - unii:ml4qrz1hcl), apomorphine (unii: n21far7b4s) (apomorphine - unii:n21far7b4s), beta-endorphin human (unii: 3s51p4w3xq) (beta-endorphin human - unii:3s51p4w3xq) - viatrexx-ithurts  a sterile, injectable, biodegradable, clear isotonic liquid that is injected into the various layers of the skin, muscles, ligaments, joints, other body tissues or added to an iv, either as a push or into the bag. this product should not be used in patients with a known hypersensitivity to any ingredient found in the formula, porcine products, isotonic saline or benzyl alcohol, or patients with a history of severe allergies. as with all injections, epinephrine injection (1:1,000) must be immediately available should an acute anaphylactoid reaction occur due to any component of the injection. this product contains 1% benzyl alcohol. benzyl alcohol has been reported to be associated with a fatal "gasping syndrome" in premature infants. due to the benzyl alcohol content, this product should not be given to a pregnant woman. this product should not be used in patients with a known hypersensitivity to any ingredient in this formula, porcine products, isotonic saline or benzyl alcohol, or patients

VIATREXX-INFLA- aconitum, anti-interleukin-1, apis, adrenal, belladonna, beta endorphin, citric acid, coelliac plexus, bryonia, USA - engelsk - NLM (National Library of Medicine)

viatrexx-infla- aconitum, anti-interleukin-1, apis, adrenal, belladonna, beta endorphin, citric acid, coelliac plexus, bryonia,

viatrexx bio incorporated - anti-interleukin-1.alpha. immunoglobulin g rabbit (unii: ml4qrz1hcl) (anti-interleukin-1.alpha. immunoglobulin g rabbit - unii:ml4qrz1hcl), aconitum napellus (unii: u0nq8555jd) (aconitum napellus - unii:u0nq8555jd), apis mellifera (unii: 7s82p3r43z) (apis mellifera - unii:7s82p3r43z), beta-endorphin human (unii: 3s51p4w3xq) (metenkefalin - unii:9jez9od3as), bos taurus adrenal gland (unii: m2776swb29) (bos taurus adrenal gland - unii:m2776swb29), sus scrofa adrenal gland (unii: 398iyq16yv) (sus scrofa adrena - viatrexx-infla  a sterile, injectable, biodegradable, clear isotonic liquid that is injected into the various layers of the skin, muscles, ligaments, joints, other body tissues or added to an iv, either as a push or into the bag. this product should not be used in patients with a known hypersensitivity to any ingredient found in the formula, porcine products, isotonic saline or benzyl alcohol, or patients with a history of severe allergies. as with all injections, epinephrine injection (1:1,000) must be immediately available should an acute anaphylactoid reaction occur due to any component of the injection. this product contains 1% benzyl alcohol. benzyl alcohol has been reported to be associated with a fatal "gasping syndrome" in premature infants. due to the benzyl alcohol content, this product should not be given to a pregnant woman. this product should not be used in patients with a known hypersensitivity to any ingredient in this formula, porcine products, isotonic saline or benzyl alcohol, or patients w

VIATREXX-LIVER- carduus benedictus, carduus marianus, ceanothus americanus, chelidonium majus, chionanthus virginica, choline, c USA - engelsk - NLM (National Library of Medicine)

viatrexx-liver- carduus benedictus, carduus marianus, ceanothus americanus, chelidonium majus, chionanthus virginica, choline, c

viatrexx bio incorporated - centaurea benedicta (unii: 6l5zl09795) (centaurea benedicta - unii:6l5zl09795), milk thistle (unii: u946sh95ee) (milk thistle - unii:u946sh95ee), ceanothus americanus leaf (unii: 25b1y14t8n) (ceanothus americanus leaf - unii:25b1y14t8n), chelidonium majus (unii: 7e889u5rnn) (chelidonium majus - unii:7e889u5rnn), chionanthus virginicus bark (unii: s9y4b22u2e) (chionanthus virginicus bark - unii:s9y4b22u2e), choline (unii: n91bdp6h0x) (choline - unii:n91bdp6h0x), bos taurus solar plexus (unii: y8h8s1x8ib) (bo - viatrexx-liver  a sterile, injectable, biodegradable, clear isotonic liquid that is injected into the various layers of the skin, muscles, ligaments, joints, other body tissues or added to an iv, either as a push or into the bag. this product should not be used in patients with a known hypersensitivity to any ingredient found in the formula, porcine products, isotonic saline or benzyl alcohol, or patients with a history of severe allergies. as with all injections, epinephrine injection (1:1,000) must be immediately available should an acute anaphylactoid reaction occur due to any component of the injection. this product contains 1% benzyl alcohol. benzyl alcohol has been reported to be associated with a fatal "gasping syndrome" in premature infants. due to the benzyl alcohol content, this product should not be given to a pregnant woman. this product should not be used in patients with a known hypersensitivity to any ingredient in this formula, porcine products, isotonic saline or benzyl alcohol, or patients w