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  2. Lamotrigine - Wikipedia

    en.wikipedia.org/wiki/Lamotrigine

    Lamotrigine is metabolized predominantly by glucuronic acid conjugation. Its major metabolite is an inactive 2-n-glucuronide conjugate. [83] Lamotrigine has fewer drug interactions than many anticonvulsant drugs, although pharmacokinetic interactions with carbamazepine, phenytoin and other hepatic enzyme-inducing medications may shorten half ...

  3. Mood stabilizer - Wikipedia

    en.wikipedia.org/wiki/Mood_stabilizer

    Lamotrigine (aka Lamictal) FDA approved for bipolar disorder maintenance therapy, not for acute mood problems like depression or mania/hypomania. [10] The usual target dose is 100–200 mg daily, titrated to by 25 mg increments every 2 weeks. [11] Lamotrigine can cause Stevens–Johnson syndrome, a very rare but potentially fatal skin condition ...

  4. Lithium (medication) - Wikipedia

    en.wikipedia.org/wiki/Lithium_(medication)

    [139] [140] Nanoparticles and microemulsions have also been invented as drug delivery mechanisms. As of 2020, there is a lack of evidence that alternate formulations or salts of lithium would reduce the need for monitoring serum lithium levels or lower systemic toxicity. [139]

  5. Lennox–Gastaut syndrome - Wikipedia

    en.wikipedia.org/wiki/Lennox–Gastaut_syndrome

    Lennox–Gastaut syndrome (LGS) is a complex, rare, and severe childhood-onset epilepsy syndrome. It is characterized by multiple and concurrent seizure types including tonic seizure, cognitive dysfunction, and slow spike waves on electroencephalogram (EEG), which are very abnormal. [1]

  6. Fluoxetine - Wikipedia

    en.wikipedia.org/wiki/Fluoxetine

    In 2019 a systematic review compared the effects on weight of various doses of fluoxetine (60 mg/d, 40 mg/d, 20 mg/d, 10 mg/d) in obese and overweight adults. [55] When compared to placebo, all dosages of fluoxetine appeared to contribute to weight loss but lead to increased risk of experiencing side effects, such as dizziness, drowsiness ...

  7. Meloxicam - Wikipedia

    en.wikipedia.org/wiki/Meloxicam

    It blocks cyclooxygenase-2 (COX-2) more than it blocks cyclooxygenase-1 (COX-1). [11] It is in the oxicam family of chemicals and is closely related to piroxicam. [11] Meloxicam was patented in 1977 and approved for medical use in the United States in 2000. [11] [13] It was developed by Boehringer Ingelheim and is available as a generic ...

  8. Mirtazapine - Wikipedia

    en.wikipedia.org/wiki/Mirtazapine

    Mirtazapine is a very strong H 1 receptor antagonist and, as a result, it can cause powerful sedative and hypnotic effects. [11] A single 15 mg dose of mirtazapine to healthy volunteers has been found to result in over 80% occupancy of the H 1 receptor and to induce intense sleepiness. [92]

  9. Scale height - Wikipedia

    en.wikipedia.org/wiki/Scale_height

    The earth atmosphere's scale height is about 8.5 km, as can be confirmed from this diagram of air pressure p by altitude h: At an altitude of 0, 8.5, and 17 km, the pressure is about 1000, 370, and 140 hPa, respectively.

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