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  2. Dog appeasing pheromone - Wikipedia

    en.wikipedia.org/wiki/Dog_appeasing_pheromone

    Dog appeasing pheromone is secreted by lactating dogs. Dog appeasing pheromone (DAP), sometimes known as apasine, is a mixture of esters of fatty acids released by the sebaceous glands in the inter-mammary sulcus of lactating female dogs. It is secreted from between three and four days after parturition and two to five days after weaning. [1]

  3. Sominex - Wikipedia

    en.wikipedia.org/wiki/Sominex

    In July 1975, the J. B. Williams Co. began marketing Sominex 2. [37] On November 24, 1975, Attorney General Evelle J. Younger filed suit on behalf of the State of California against Williams Co., stating that the product did not warn against use by pregnant or nursing women or persons with asthma or COPD, nor did it notify consumers that it should not be used in conjunction with alcohol. [38]

  4. Potassium bromide - Wikipedia

    en.wikipedia.org/wiki/Potassium_bromide

    The product is intended to be used in dogs, primarily as an antiepileptic (to stop seizures). [5] The pink color of the solution is artificial; pure potassium bromide solutions are colorless The anticonvulsant properties of potassium bromide were first noted by Sir Charles Locock at a meeting of the Royal Medical and Chirurgical Society in 1857.

  5. Holland & Barrett - Wikipedia

    en.wikipedia.org/wiki/Holland_&_Barrett

    Holland & Barrett, King Street, Hammersmith, London Holland & Barrett International Limited, trading as Holland & Barrett (H&B), is a British-based multinational chain of health food shops with over 1,300 stores in 16 countries, including a substantial presence in the United Kingdom, Republic of Ireland, Netherlands, Belgium, Mainland China, Hong Kong, India, Saudi Arabia, Lithuania and UAE.

  6. Butorphanol - Wikipedia

    en.wikipedia.org/wiki/Butorphanol

    Butorphanol is available as the tartrate salt in injectable, tablet, and intranasal spray formulations. The tablet form is only used in dogs, cats and horses due to low bioavailability in humans. It was patented in 1971 and approved for medical use in 1979.

  7. Oclacitinib - Wikipedia

    en.wikipedia.org/wiki/Oclacitinib

    Oclacitinib lacks the side effects that most JAK inhibitors have in humans; instead, side effects are infrequent, mild, and mostly self-limiting. [13] [14] [16] The most common side effects are gastrointestinal problems (vomiting, diarrhea, and appetite loss) and lethargy. The GI problems can sometimes be alleviated by giving oclacitinib with food.