Patent classifications
A61K31/397
Mechanochemcial activated dry amorphisation by milling equilibrium between AP mesoporous silica
Particles are disclosed. Methods of making and using the particles are also disclosed.
Mechanochemcial activated dry amorphisation by milling equilibrium between AP mesoporous silica
Particles are disclosed. Methods of making and using the particles are also disclosed.
METHODS AND COMPOSITIONS FOR TREATING CANNABINOID OVERDOSE WITH A CANNABINOID RECEPTOR ANTAGONIST
Disclosed herein are formulations and methods for reversing one or more symptoms of cannabinoid overdose, comprising parenterally administering a CB1 antagonist in an amount sufficient to reverse the cannabinoid overdose symptoms.
METHODS AND COMPOSITIONS FOR TREATING CANNABINOID OVERDOSE WITH A CANNABINOID RECEPTOR ANTAGONIST
Disclosed herein are formulations and methods for reversing one or more symptoms of cannabinoid overdose, comprising parenterally administering a CB1 antagonist in an amount sufficient to reverse the cannabinoid overdose symptoms.
METHODS OF TREATMENT
The present disclosure provides for methods of treating a patient with a CYP3A4 substrate drug, wherein the patient is treated with posaconazole. In some embodiments, the patient stops posaconazole treatment, waits for at least 2 days, and then is treated with the CYP3A4 substrate drug as soon as it is safe to do so. In some embodiments, treatment with the CYP3A4 substrate drug is delayed for about 2-42 days after stopping posaconazole. In some embodiments, the patient is treated with a reduced dose of the CYP3A4 substrate drug for about 2-42 days.
METHODS OF TREATMENT
The present disclosure provides for methods of treating a patient with a CYP3A4 substrate drug, wherein the patient is treated with posaconazole. In some embodiments, the patient stops posaconazole treatment, waits for at least 2 days, and then is treated with the CYP3A4 substrate drug as soon as it is safe to do so. In some embodiments, treatment with the CYP3A4 substrate drug is delayed for about 2-42 days after stopping posaconazole. In some embodiments, the patient is treated with a reduced dose of the CYP3A4 substrate drug for about 2-42 days.
Combinations of beta-lactam compounds and probenecid and uses thereof
The present disclosure relates to bilayer tablets comprising a second layer comprising a β-lactam compound or a pharmaceutically acceptable salt thereof; and a first layer comprising probenecid or a pharmaceutically acceptable salt thereof. The present disclosure also relates to methods of treating or preventing a disease using the bilayer tablets.
Combinations of beta-lactam compounds and probenecid and uses thereof
The present disclosure relates to bilayer tablets comprising a second layer comprising a β-lactam compound or a pharmaceutically acceptable salt thereof; and a first layer comprising probenecid or a pharmaceutically acceptable salt thereof. The present disclosure also relates to methods of treating or preventing a disease using the bilayer tablets.
COMPOSITIONS FOR THE TREATMENT OF HYPERTENSION
Provided herein are pharmaceutical compositions that are useful for the treatment of hypertension comprising an angiotensin II receptor blocker, a diuretic, and a calcium channel blocker.
COMPOSITIONS FOR THE TREATMENT OF HYPERTENSION
Provided herein are pharmaceutical compositions that are useful for the treatment of hypertension comprising an angiotensin II receptor blocker, a diuretic, and a calcium channel blocker.