Middle Ear Infection Research Dashboard
Double-blind human trials
Clinical human trials
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CannaKeys has 2 studies associated with Middle Ear Infection.
Here is a small sampling of Middle Ear Infection studies by title:
- Antifungal action of α-pinene against Candida spp. isolated from patients with otomycosis and effects of its association with boric acid
- Therapeutic effects of borneol-walnut oil in the treatment of purulent otitis media.
Components of the Middle Ear Infection Research Dashboard
- Dosing information available for Middle Ear Infection
- Chemotype guidance for treating Middle Ear Infection with cannabis
- Synopsis of cannabis research for Middle Ear Infection
- Individual study details for Middle Ear Infection
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Overview - Middle Ear Infection
Description of Middle Ear Infection
Otitis Media is an umbrella term used to describe three types of inflammatory diseases that affect the middle ear. One, acute otitis media (AOM) has a sudden onset with significant pain, while otitis media with effusion (OME) presents often without pain or with a little discomfort but with discharge, and the third version is chronic suppurative otitis media (CSOM). Each of these condition bring with them the potential of hearing loss. Infectious causes include viral or bacterial infections, and other causes include allergic responses, and trauma for example. Pharmaceutical drugs used to treat middle ear infections depend on underlying cause and may include analgesia, antibiotics, or antihistamines for instance. Other orthodox treatments methods may include the insertion of a tube into the ear canal.
Middle Ear Infection
Diseases of the Ear and Mastoid Process
ICD-10 Code: H66
Middle Ear Infection Symptoms:
Ear pain (in AOM), discharge (from the ear in cases of OME), chronic inflammation (CSOM), fever (esp. in infants)
Also known as:
THC Interaction with Pharmaceutical Drugs
- THC can enhance the effects of drugs that cause sedation and depress the central nervous system, such as benzodiazepines, barbiturates, and alcohol, for example.
- THC is metabolized by and an inhibitor of a number of enzymatic liver pathways referred to as cytochrome P450. There are more than 50 enzymes belonging to this enzyme family, a number of which are responsible for the breakdown of common drugs such as antidepressants (e.g. amitriptyline, doxepine, fluvoxamine), antipsychotics (haloperidol, clozapine, stelazine), beta-blockers (e.g. propranolol), bronchodilators (e.g. theophylline), or bloodthinners (e.g. warfarin). Thus patients taking these classes of medication may find that THC increases the concentration and effects of these drugs as well as the duration of their effects.
- Clinical observation suggests no likely interactions with other pharmaceuticals at a total daily dose of up to 20mg THC.
CBD Interaction with Pharmaceutical Drugs
- CBD may alter action on metabolic enzymes (certain drug-transport mechanisms), and as such may alter interactions with other drugs, some of which may produce therapeutic or adverse effects. For instance, CBD interacts with the enzyme cytochrome P450 3A4 and cytochrome P450 2C19, increasing the bioavailability of anti-epileptic drugs such as clobazam (a benzodiazepine). This makes it possible to achieve the same results at significantly lower dosages, reducing treatment costs and risks of adverse effects.
- Groups of drugs affected include: anti-epileptic drugs, psychiatric drugs, and drugs affecting metabolic enzymes, for example.
- Clinical observations suggest no likely interactions with other pharmaceuticals at a total daily dose of up to 100mg CBD
THC Dosage Considerations
- THC micro dose: 0.1 mg to 0.4 mg
- THC low dose: 0.5 mg to 5 mg
- THC medium dose: 6 mg to 20 mg
- THC high dose: 21 mg to 50+ mg
CBD Dosage Considerations
- CBD low dose: 0.4 mg to 19 mg
- CBD medium dose: 20 mg to 99 mg
- CBD high dose: 100 mg to 800+ mg (upper limits tested ~1,500mg)
Disclaimers: Information on this site is provided for informational purposes only and is not meant to substitute for the advice provided by your own physician or other medical professional. You should not use the information contained herein for diagnosing a health problem or disease. If using a product, you should read carefully all product packaging. If you have or suspect that you have a medical problem, promptly contact your health care provider.
Information on this site is based on scientific studies (human, animal, or in vitro), clinical experience, or traditional usage as cited in each article. The results reported may not necessarily occur in all individuals. For many of the conditions discussed, treatment with prescription or over-the-counter medication is also available. Consult your physician, nutritionally oriented health care practitioner, and/or pharmacist for any health problem and before using any supplements or before making any changes in prescribed medications.