Spojené státy - angličtina - NLM (National Library of Medicine)

physicians total care, inc. - diclofenac sodium (unii: qtg126297q) (diclofenac - unii:144o8ql0l1) - diclofenac sodium 25 mg - carefully consider the potential benefits and risks of diclofenac sodium delayed-release tablets and other treatment options before deciding to use diclofenac sodium delayed-release tablets. use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see warnings ). diclofenac sodium delayed-release tablets, are indicated: - for relief of signs and symptoms of osteoarthritis - for relief of signs and symptoms of rheumatoid arthritis - for acute or long-term use in the relief of signs and symptoms of ankylosing spondylitis diclofenac sodium delayed-release tablets, are contraindicated in patients with known hypersensitivity to diclofenac. diclofenac sodium delayed-release tablets should not be given to patients who have experienced asthma, urticaria, or other allergic-type reactions after taking aspirin or other nsaids. severe, rarely fatal, anaphylactic-like reactions to nsaids have been reported in such patients (see warnings: anaphylactoid reactions

Spojené státy - angličtina - NLM (National Library of Medicine)

physicians total care, inc. - clonazepam (unii: 5pe9fde8gb) (clonazepam - unii:5pe9fde8gb) - clonazepam 0.25 mg - clonazepam is useful alone or as an adjunct in the treatment of the lennox-gastaut syndrome (petit mal variant), akinetic and myoclonic seizures. in patients with absence seizures (petit mal) who have failed to respond to succinimides, clonazepam may be useful. in some studies, up to 30% of patients have shown a loss of anticonvulsant activity, often within 3 months of administration. in some cases, dosage adjustment may reestablish efficacy. clonazepam is indicated for the treatment of panic disorder, with or without agoraphobia, as defined in dsm-iv. panic disorder is characterized by the occurrence of unexpected panic attacks and associated concern about having additional attacks, worry about the implications or consequences of the attacks, and/or a significant change in behavior related to the attacks. the efficacy of clonazepam was established in two 6- to 9-week trials in panic disorder patients whose diagnoses corresponded to the dsm-iiir category of panic disorder (see clinical pharmacology: clinical

Spojené státy - angličtina - NLM (National Library of Medicine)

physicians total care, inc. - metoclopramide hydrochloride (unii: w1792a2rvd) (metoclopramide - unii:l4yeb44i46) - metoclopramide 5 mg - the use of metoclopramide tablets is recommended for adults only. therapy should not exceed 12 weeks in duration. metoclopramide tablets are indicated as short-term (4 to 12 weeks) therapy for adults with symptomatic, documented gastroesophageal reflux who fail to respond to conventional therapy. the principal effect of metoclopramide is on symptoms of postprandial and daytime heartburn with less observed effect on nocturnal symptoms. if symptoms are confined to particular situations, such as following the evening meal, use of metoclopramide as single doses prior to the provocative situation should be considered, rather than using the drug throughout the day. healing of esophageal ulcers and erosions has been endoscopically demonstrated at the end of a 12-week trial using doses of 15 mg q.i.d. as there is no documented correlation between symptoms and healing of esophageal lesions, patients with documented lesions should be monitored endoscopically. metoclopramide tablets, are indicated for the re

Spojené státy - angličtina - NLM (National Library of Medicine)

physicians total care, inc. - ibuprofen (unii: wk2xyi10qm) (ibuprofen - unii:wk2xyi10qm) - ibuprofen 100 mg in 5 ml - in pediatric patients , : - for reduction of fever in patients aged 6 months up to 2 years of age. - for relief of mild to moderate pain in patients aged 6 months up to 2 years of age. - for relief of signs and symptoms of juvenile arthritis. in adults , : - for treatment of primary dysmenorrhea. - for relief of the signs and symptoms of rheumatoid arthritis and osteoarthritis. carefully consider the potential benefits and risks of ibuprofen suspension and other treatment options before deciding to use ibuprofen suspension. use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see warnings ). in pediatric patients , ibuprofen suspension is indicated: - for reduction of fever in patients aged 6 months up to 2 years of age. - for relief of mild to moderate pain in patients aged 6 months up to 2 years of age. - for relief of signs and symptoms of juvenile arthritis. in adults , ibuprofen is indicated: - for treatment of primary dysmenorrhea. - for reli

Spojené státy - angličtina - NLM (National Library of Medicine)

physicians total care, inc. - zonisamide (unii: 459384h98v) (zonisamide - unii:459384h98v) - zonisamide 50 mg - zonisamide is indicated as adjunctive therapy in the treatment of partial seizures in adults with epilepsy. zonisamide is contraindicated in patients who have demonstrated hypersensitivity to sulfonamides or zonisamide. the abuse and dependence potential of zonisamide has not been evaluated in human studies (see warnings, cognitive/neuropsychiatric adverse events subsection). in a series of animal studies, zonisamide did not demonstrate abuse liability and dependence potential. monkeys did not self-administer zonisamide in a standard reinforcing paradigm. rats exposed to zonisamide did not exhibit signs of physical dependence of the cns-depressant type. rats did not generalize the effects of diazepam to zonisamide in a standard discrimination paradigm after training, suggesting that zonisamide does not have abuse potential of the benzodiazepine-cns depressant type.

Spojené státy - angličtina - NLM (National Library of Medicine)

physicians science and nature, inc. - methyl salicylate 25.00%, menthol 15.00%, capsaicin 0.1%, topical analgesic - for temporary relief of minor aches and pains of muscles and joints associated with arthritis, simple backache, sprains and strains. does not prevent or cure any disease. on cuts, infected skin or over raw or blistered skin, on children under 12 years of age or pets, in large amount, if allergic to any of the listed ingredients, including cannabinoids/cannibidiol or aspirin products, if you are pregnant or nursing, taking anticoagulant medications, if suffering with parkinson's disease or severe psychiatric disease. if you have any questions regarding the safe use of this medication, please contact your medical provider. for severe undiagnosed pain. if pain worsens or persists for more than 7 days. if pain clears up and then recurs in a few days. if itching or skin rash occurs. if any other advierse effects occur.

Spojené státy - angličtina - NLM (National Library of Medicine)

physicians science and nature, inc. - methyl salicylate 25.00%, menthol 15.00%, capsaicin 0.1%, topical analgesic - for temporary relief of minor aches and pains of muscles and joints associated with arthritis, simple backache, sprains and strains. does not prevent or cure any disease. on cuts, infected skin or over raw or blistered skin, on children under 12 years of age or pets, in large amount, if allergic to any of the listed ingredients, including cannabinoids/cannibidiol or aspirin products, if you are pregnant or nursing, taking anticoagulant medications, if suffering with parkinson's disease or severe psychiatric disease. if you have any questions regarding the safe use of this medication, please contact your medical provider. for severe undiagnosed pain. if pain worsens or persists for more than 7 days. if pain clears up and then recurs in a few days. if itching or skin rash occurs. if any other advierse effects occur. ​power pain relief stick with broad-spectrum hemp extract ​contains 300mg cbd thc free recommended by physicians hypoallergenic deep penetrating action 3 ounces (85 gm) - ndc 27495-022-03

Austrálie - angličtina - APVMA (Australian Pesticides and Veterinary Medicines Authority)

corteva agriscience australia pty ltd - clopyralid present as the potassium salt - water soluble granules - clopyralid present as the potassium salt pyridine active 750.0 g/kg - herbicide - canola - post emergence | canola - post sowing/pre-emergence | canola (prior to sowing) | canola-triazine tolerant only-post eme - californian thistle | canola - brassica napus | capeweed | common cotula or carrot weed | cotulas | creeping/russian knapweed,hardhead | lucerne | nodding thistle | prickly lettuce | saffron thistle | scotch thistle | skeleton weed | slender, shore or sheep thistle | soldier thistle | sow or milk thistle | spear or black thistle | st barnaby's thistle | stemless thistle | subterranean clover | variegated thistle | vetches | volunteer chickpea | volunteer faba bean | volunteer field pea | volunteer lentil | volunteer lucerne - seedling | volunteer lupin | volunteer medic | volunteer safflower | volunteer subterranean clover | volunteer vetch or tares | bird's eye | blessed thistle | bull thistle | cabbage thistle | canada thistle | carduus marianus | common lucerne | common sowthistle | cotton thistle | creeping thistle | false star thistle | field pea | hairy vetch | hardhead thistle | heraldic thistle | holy thistle | lady's thistle | lentil | milk thistle | musk thistle | narrowleaf vetch | perennial thistl

Austrálie - angličtina - APVMA (Australian Pesticides and Veterinary Medicines Authority)

bayer cropscience pty ltd - triflumuron - suspension concentrate - triflumuron uron active 480.0 g/l - insecticide - mushroom - sciarid fly | bradysia spp.

Austrálie - angličtina - APVMA (Australian Pesticides and Veterinary Medicines Authority)

bayer cropscience pty ltd - penflufen; trifloxystrobin - suspension concentrates for seed treatment (fs) - penflufen pyrazole active 154.0 g/l; trifloxystrobin strobiluron active 154.0 g/l - fungicide - canola | rapeseed - damping off | rhizoctonia solani | damping off | fusarium spp. | hypocotyl rot | sclerotinia spp.