CODEIN SLOVAKOFARMA 15MG Tableta Tsjekkia - tsjekkisk - SUKL (Státní ústav pro kontrolu léčiv)

codein slovakofarma 15mg tableta

zentiva, k.s., praha array - 5382 hemihydrÁt kodein-fosfÁtu - tableta - 15mg - kodein

CODEIN SLOVAKOFARMA 30MG Tableta Tsjekkia - tsjekkisk - SUKL (Státní ústav pro kontrolu léčiv)

codein slovakofarma 30mg tableta

zentiva, k.s., praha array - 5382 hemihydrÁt kodein-fosfÁtu - tableta - 30mg - kodein

CODEINE SULFATE tablet USA - engelsk - NLM (National Library of Medicine)

codeine sulfate tablet

lannett company, inc. - codeine sulfate (unii: 11qv9bs0cb) (codeine anhydrous - unii:ux6owy2v7j) - codeine sulfate 15 mg - codeine sulfate tablets are indicated for the management of mild to moderate pain, where treatment with an opioid is appropriate and for which alternative treatments are inadequate. limitations of use because of the risks of addiction, abuse, and misuse with opioids, even at recommended doses [ s ee warnings and precautions ( 5.1 ) ] , reserve codeine sulfate tablets for use in patients for whom alternative treatment options [e.g., non-opioid analgesics or opioid combination products]: - have not been tolerated, or are not expected to be tolerated. have not been tolerated, or are not expected to be tolerated. - have not provided adequate analgesia, or are not expected to provide adequate analgesia. have not provided adequate analgesia, or are not expected to provide adequate analgesia. codeine sulfate tablets are contraindicated for: - all children younger than 12 years of age [see warnings and precautions ( 5.4 )] . - post-operative management in children younger than 18 years of age following tonsillect

CODEINE AND CHLORPHENIRAMINE MALEATE ER tablet, extended release USA - engelsk - NLM (National Library of Medicine)

codeine and chlorpheniramine maleate er tablet, extended release

nexgen pharma, inc. - codeine phosphate (unii: gsl05y1mn6) (codeine anhydrous - unii:ux6owy2v7j), chlorpheniramine maleate (unii: v1q0o9oj9z) (chlorpheniramine - unii:3u6io1965u) - codeine phosphate 54.3 mg - codeine phosphate and chlorpheniramine maleate is indicated for the relief of cough and symptoms associated with upper respiratory allergies or a common cold in adults 18 years of age and older. important limitations of use not indicated for pediatric patients under 18 years of age [see use in special population (8.4)] patients with known hypersensitivity to codeine, chlorpheniramine or any of the inactive ingredients of codeine phosphate and chlorpheniramine maleate. persons known to be hypersensitive to certain other opioids may exhibit cross-sensitivity to codeine. teratogenic effects pregnancy category c there are no adequate and well-controlled studies of codeine phosphate and chlorpheniramine maleate in pregnant women. reproductive toxicity studies have not been conducted with codeine phosphate and chlorpheniramine maleate; however, studies are available with individual active ingredients or related active ingredients. because animal reproduction studies are not always predictive of human response, co

CODEINE SULFATE tablet USA - engelsk - NLM (National Library of Medicine)

codeine sulfate tablet

physicians total care, inc. - codeine sulfate (unii: 11qv9bs0cb) (codeine - unii:q830pw7520) - codeine sulfate 60 mg - codeine sulfate is an opioid analgesic indicated for the relief of mild to moderately severe pain where the use of an opioid analgesic is appropriate. codeine sulfate is contraindicated in patients with known hypersensitivity to codeine or any components of the product. persons known to be hypersensitive to certain other opioids may exhibit cross-sensitivity to codeine. codeine sulfate is contraindicated in patients with respiratory depression in the absence of resuscitative equipment. codeine sulfate is contraindicated in patients with acute or severe bronchial asthma or hypercarbia. codeine sulfate is contraindicated in any patient who has or is suspected of having paralytic ileus. enter section text here codeine sulfate is an opioid agonist and is a schedule ii controlled substance. codeine sulfate can be abused and is subject to criminal diversion.  drug addiction is characterized by compulsive use, use for non-medical purposes, and continued use despite harm or risk of harm. drug addiction is

PARACETAMOL/CODEINE VIATRIS 500 mg/30 mg, comprimé Frankrike - fransk - ANSM (Agence Nationale de Sécurité du Médicament et des Produits de Santé)

paracetamol/codeine viatris 500 mg/30 mg, comprimé

viatris sante - phosphate de codéine hémihydraté 30 mg; paracétamol 500 mg - comprimé - 30 mg - pour un comprimé > phosphate de codéine hémihydraté 30 mg > paracétamol 500 mg - antalgiques. opioïdes en association avec des antalgiques non-opioïdes. codéine et paracétamol - paracetamol/codeine viatris contient deux antalgiques (antidouleurs) appelés paracétamol et codéine (sous forme de phosphate de codéine hémihydraté). la codéine appartient à un groupe de médicaments appelés les antalgiques opioïdes qui agissent pour soulager la douleur.paracetamol/codeine viatris peut être utilisé chez les enfants âgés de plus de 12 ans pour le soulagement à court terme des douleurs modérées qui ne sont pas soulagées par d’autres antalgiques comme le paracétamol ou l’ibuprofène utilisés seuls.

Codeinoform Qualiphar 10 mg/15 ml sirop Belgia - fransk - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

codeinoform qualiphar 10 mg/15 ml sirop

laboratoria qualiphar sa-nv - codéine 10 mg/15 ml - sirop - 10 mg/15 ml - codéine 0.5 mg/g - codeine

Codeinoform Qualiphar 10 mg/15 ml siroop Belgia - nederlandsk - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

codeinoform qualiphar 10 mg/15 ml siroop

laboratoria qualiphar sa-nv - codeïne 10 mg/15 ml - siroop - 10 mg/15 ml - codeïne 0.5 mg/g - codeine

DIHYDROCODEINE BITARTRATE, ACETAMINOPHEN AND CAFFEINE tablet USA - engelsk - NLM (National Library of Medicine)

dihydrocodeine bitartrate, acetaminophen and caffeine tablet

physicians total care, inc. - dihydrocodeine bitartrate (unii: 8lxs95bsa9) (dihydrocodeine - unii:n9i9hdb855), acetaminophen (unii: 362o9itl9d) (acetaminophen - unii:362o9itl9d), caffeine (unii: 3g6a5w338e) (caffeine - unii:3g6a5w338e) - dihydrocodeine bitartrate 32 mg - acetaminophen, caffeine, and dihydrocodeine bitartrate tablets are indicated for the relief of moderate to moderately severe pain. this combination product is contraindicated in persons with hypersensitivity to dihydrocodeine, codeine, acetaminophen, caffeine, or any of the inactive components listed above, or any situation where opioids are contraindicated including significant respiratory depression (in unmonitored settings or in the absence of resuscitative equipment), acute or severe bronchial asthma or hypercapnia, and paralytic ileus. this combination product is subject to the provisions of the controlled substance act, and has been placed in schedule iii. dihydrocodeine can produce drug dependence of the codeine type and therefore has the potential of being abused. like other opioid analgesics, dihydrocodeine may produce subjective effects other than analgesia (e.g., euphoria, relaxation), which may contribute to abuse by some patients. psychological dependence, physical dependence, and tolerance may d