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Reminyl (Galantamine)
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Reminyl

Reminyl is used to treat mild to moderate confusion (dementia) related to Alzheimer's disease. It does not cure Alzheimer's disease, but it may improve memory, awareness, and the ability to perform daily functions. This medication works by restoring the balance of certain natural substances (neurotransmitters) in the brain.

Other names for this medication:
Galamer, Galantamine, Razadyne

Similar Products:
Colcrys, Panadol, Benemid, Priligy, Vermox, Fulvicin, Feldene, Addyi, Coreg

Also known as: Galantamine

Description

{name}-D 12 Hour contains a combination of desloratadine and pseudoephedrine. Desloratadine is an antihistamine that reduces the effects of natural chemical histamine in the body. Histamine can produce symptoms of sneezing, itching, watery eyes, and runny nose.

Pseudoephedrine is a decongestant that shrinks blood vessels in the nasal passages. Dilated blood vessels can cause nasal congestion (stuffy nose).

{name}-D 12 Hour is used to treat sneezing, runny or stuffy nose, itchy or watery eyes, hives, skin rash, itching, and other symptoms of allergies and the common cold.

{name}-D 12 Hour is for adults and children who are at least 12 years old.

Dosage

Take Reminyl Plus D exactly as it was prescribed for you. Follow all directions on your prescription label. Do not take this medicine in larger or smaller amounts or for longer than recommended.

Reminyl Plus D tablets are taken once each week. Choose the day of the week that best fits your schedule. Every week, take one Reminyl Plus D tablet on your chosen day.

Take the Reminyl Plus D tablet first thing in the morning, at least 30 minutes before you eat or drink anything or take any other medicine.

Take the tablet with a full glass (6 to 8 ounces) of water. Use only plain water (not mineral water) when taking this medicine.

Do not crush, chew, or suck the tablet. Swallow the pill whole.

After taking an Reminyl Plus D tablet, carefully follow these instructions:

Do not lie down or recline for at least 30 minutes after taking Reminyl Plus D. Do not eat or drink anything other than plain water. Do not take any other medicines including vitamins, calcium, or antacids for at least 30 minutes after taking Reminyl Plus D. It may be best to take your other medicines at a different time of the day. Talk with your doctor about the best dosing schedule for your other medicines.

To be sure this medication is helping your condition, your bone mineral density will need to be tested on a regular basis. You may not need to take Reminyl Plus D for longer than 3 to 5 years if you take it for osteoporosis.

If you need to have any dental work (especially surgery), tell the dentist ahead of time that you are using Reminyl Plus D. You may need to stop using the medicine for a short time.

Reminyl Plus D is only part of a complete program of treatment that may also include diet changes, exercise, and taking calcium and vitamin supplements. Follow your diet, medication, and exercise routines very closely.

Store at room temperature away from moisture and heat.

Detailed Reminyl Plus D dosage information

Overdose

If you overdose Generic Reminyl and you don't feel good you should visit your doctor or health care provider immediately.

Storage

Store at room temperature between 15 and 30 degrees C (59 and 86 degrees F) away from moisture and heat. Throw away any unused medicine after the expiration date. Keep out of the reach of children.

Side effects

The most common side effects associated with Reminyl are:

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Insulin stimulation revealed robust relationships between human plasma BCAA and indices of insulin resistance, indicating chronic metabolic overload from BCAA. Case report of anticonvulsant hypersensitivity syndrome complicated by a concomitant atypical pneumonia. In traditional teaching, it has been characterised as almost pathognomonic of a lesion in the subthalamic nucleus (STN). Capsid, membrane and NS3 are the major viral proteins involved in autophagy induced by Japanese encephalitis virus. The aim of the current study was, therefore, to examine potential relationships between the social background of Japanese working-age individuals affected by the 2013 voluntary vaccination campaign.

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