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Acetaminophen (Tylenol)

Tylenol is a drug brand in North America that reduces fever and pain and relieves the symptoms of flu, cough, cold and certain allergies. The active ingredient of this drug is acetaminophen, an antipyretic and analgesic drug.

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What is difference between midol and say Tylenol for example?

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in addition to pain reliever, Midol also contains a diuretic. Tylenol is strictly a pain reliever (or fever reducer)

Can you use acetaminophen tablets for cats?

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No, you cannot give Tylenol to cats for pain because it can cause a fatal reaction (Heinz body anemia). Even a single pill is far too much and could kill your cat.

This is why you should never give people medication to pets - they are not small humans and what would be safe for you may be lethal to them.

What should you do if your dog ate a mouse?

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Your dog can bleed to death over a few days if not helped asap. The ingredients in mouse/rat poison are designed to stop the blood from clotting, this will happen to your dog too. Go to the vet now and don't look for other answers that involve home remedies. GO TO THE VET!

Will baby aspirin hurt your cat?

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Never, ever, EVER give 'human' medicine to animals without consulting a qualified vet ! You have no way of determining what is a 'safe' dose or whether the animal in question would suffer any side effects.

What part of a teaspoon is 1.875 ml?

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The volume of 1 milliliter (mL) is identical to 1 cubic centimeter (cc).

1 teaspoon is 4.92892159 milliliters.

Metrificated values:

1/4 teaspoon = 1.25 ml

1/2 teaspoon = 2.5 ml

3/4 teaspoon = 3.75 ml

1 teaspoon = 5 ml

xxx 1 and 1/2 teaspoon = 7.5 ml

1 tablespoon = 15 ml

0.6 ml is how many teaspoons?

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.99 oz

1 ounce = 6 teaspoons

1 teaspoon = 0.16 ounce

One eighth of a teaspoon is equal to how many ml?

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(one eighth) of (1 US fluid ounce) = 3.6966912 millilitres

How many teaspoons is 1.75 ml?

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1.75mL equates to 0.36 (0.3550472) US teaspoons.

Can you take Tylenol after you take apple cider vinegar tonic?

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Funny, I just taked with my doctor about this. I'm going in for surgery, and she said that detoxing the liver is OK when you're taking tylenol. She mentioned that the only risks with Tylenol (acetaminophen, to be exact) is liver DAMAGE. Apple cider vinegar help the liver, so it more or less balances it out.

Hope that helps!

How many drops in 2 oz?

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This question is near impossible to answer since to properly answer it one would need to know what type of liquid is in question and what definition of drop was being used. The following are different "types" of drops:

There are several exact definitions of a "drop":

the "metric" drop, 1/20 mL (50 μL).

the medical drop, 1/12 mL (83⅓ μL).

the Imperial drop, 1/36 of a fluidram (1/288 of an Imperial fluid ounce, or 1/1440 of a gill) (approximately 99 μL).

an alternate, possibly apocryphal, definition of the drop is 1/1824 of a gill (approximately 78 μL).

the U.S. drop, 1/60 of a US fluidram, 1/80 of a teaspoon or 1/480 of a U.S. fluid ounce (approximately 62 μL).

an alternate definition of the U.S. drop is 1/96 of a teaspoon or 1/576 US fl oz (approximately 51 μL).

Can you mix childrens Tylenol with ginger ale?

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Yes I do it every time my son needs meds and it works every time. Dosage of whatever medicine with small amount of juice. You can also crush up some chewables and mix it in yogurt, ice cream, applesauce or whatever they want if the apple juice trick doesn't work

How many teaspoons are in 7 ml?

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Consider that a Teaspoon is 4.92892159 milliliters, that give you at almost 2 teaspoons for 7 ml. Rather than using a teaspoon, I would go to your local drug store and purchase a pediatric measuring device. They usually go to 30 ml and give very accurate measurements. Better safe than sorry and for just a few bucks, can save a log of headaches in trying to figure out the conversions of such ridiculously long numbers.

What does 5 ml's equal in teaspoons?

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Indeed, it seems to be that 1 teaspoon equals to 5 milliliters.

And 1 table spoon equals 15 milliliters.

How much is 8.6 milliliter in teaspoon?

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A teaspoon is 5ml. So 8.5 ml is 1 and 2/3 teaspoons, approximately.

How many ml in a tsp?

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Three teaspoons is about 14.79 milliliters.

Is paracetamol addictive?

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Paracetamol, known as acetaminophen in the United States, is a painkiller that is popular throughout the world because it is remarkably safe and it does not irritate the stomach. Paracetamol was first discovered to have both analgesic and antipyretic properties in the late nineteenth century. Prior to this, cinchona bark, which was also used to make the anti-malaria drug quinine, had been used to treat fevers. As cinchona became scarcer, people began to look for cheaper synthetic alternatives. Two of these alternative compounds were acetanilide and phenacetin, developed in 1886 and 1887 respectively. By this time, Harmon Northrop Morse had already synthesized acetaminophen in 1878 through the reduction of p-nitrophenol with tin in glacial acetic acid.

In 1893, the white, odourless crystalline compound with a bitter taste that became known as paracetamol was discovered. Initially, paracetamol was found in the urine of patients who had taken phenacetin and in 1889 it was demonstrated that paracetamol was a urinary metabolite of acetanilide. These discoveries, however, failed to attract much attention and were largely ignored at the time.

It was not until 1948, when Brodie and Axelrod established that paracetamol was a major metabolite of both acetanilide and phenacetin, that paracetamol experienced a resurgence of interest. As a derivative of p-aminophenol, paracetamol corresponds to the active principal metabolite phenacetin. It was commonly assumed at the time that their rapid conversion by the body into paracetamol was actually responsible for the therapeutic effects of both of these medicines. It was eventually ascertained that phenacetin had its own pharmacological action and was not dependent on paracetamol for its effects. Because a high proportion of phenacetin is converted into paracetamol in the liver, however, phenacetin required a large dosage to achieve any direct analgesic effect.

In 1956, 500mg tablets of paracetamol went on sale in the United Kingdom and its popularity as an over-the-counter analgesic rapidly increased. This popularity was partly explained by the fact that paracetamol was proven to be easier on the stomach than some other analgesics. Paracetamol gradually became combined with both analgesics and oral decongestants.

Paracetamol works as a weak prostaglandin inhibitor. It achieves this by blocking the production of prostaglandins, which are chemicals involved in the transmission of the pain message to the brain. In this regard, paracetamol is different from Aspirin and NSAIDs (non-steroidal anti-inflammatory drugs) in that it blocks the pain message at the brain and not at the source of the pain, as the others do.

Structually, paracetamol is similar to aspirin. They are both recognised by the same enzyme, which is called cyclo-oxygenase (COX). Cyclo-oxygenase serves as a pain activator, amplifying the degree of pain experienced in order to let the body know that there is a problem. It is this enzyme that is responsible for the biosynthesis of prostoglandins. By reducing the amount of prostaglandin available for synthesis, paracetamol helps relieve headache pain by reducing the dilation of the blood vessels that cause the pain. Paracetamol, however, only inhibits prostaglandin biosynthesis in the central nervous system (CNS) with little or no effect on peripheral tissues.

Paracetamol is used to relieve mild to moderate pain, including instances of tension headache, migraine headache, muscular aches, neuralgia, backache, joint pain, rheumatic pain, general pain, toothache, teething pain, and period pain. It is suitable for most people, including the elderly and young children, because it has very few side effects. Paracetamol is used to treat osteoarthritis, a type of non-inflammatory arthritis due to the "wear and tear" of the joints, because of its analgesic properties and its lack of gastrointestinal side effects. It can also help with the pain experienced by sufferers of arthritis.

Paracetamol is an antipyretic that can reduce fever by affecting the part of the brain known as the hypothalamus that regulates the temperature of the body. This is why paracetamol is included in many cough, cold and flu medications. Specifically, paracetamol has been given to children after they have been given vaccinations in order to prevent them developing post-immunisation pyrexia, or fever.

Paracetamol can be used by patients for whom NSAIDs are contraindicated, including those with asthma or peptic ulcers. Because there are few interactions with other medications, paracetamol can be taken by people with sensitivity to aspirin. Cholestyramine, which lowers high cholesterol, may reduce the rate at which paracetamol is absorbed by the gut, while Metoclopramide and Domperidone, which are used to relieve the symptoms of stomach disorders, may have the opposite effect and should be used with caution. Paracetamol has shown no propensity to be addictive, even in people who use it frequently. Long-term or regular use of paracetamol may, however, increase the anticoagulant activity of warfarin or similar anticoagulant medicines so caution may be required in these instances.

Some research suggests that it may protect the arteries from the changes that lead to hardening of the arteries, which can cause strokes, heart attacks or cardiovascular disease. This is because paracetamol can inhibit the oxidation of some of the low-density lipoproteins that carry 'bad' cholesterol, counteracting the process that causes the formation of arterial plaque. There is also some evidence to suggest that paracetamol may offer some protection against ovarian cancer.

Paracetamol, however, is not useful in reducing inflammation or the swelling of the skin or joints. This is because paracetamol has no clinically useful anti-inflammatory properties.

The body rapidly absorbs Paracetamol, with the soluble form being absorbed even faster than the solid tablets. As the paracetamol is metabolised, the peak blood level remains less than 20mg/litre after a standard adult 1000mg dose. Blood serum levels will normally peak between half an hour to two hours after ingestion. The analgesic properties of paracetamol will last for around four hours. Paracetamol has a half-life of about two hours, after which it will rapidly be expelled from the body.

Paracetamol is primarily metabolised in the liver. Paracetamol and its two primary metabolites are remarkably safe compounds. About 90% of the dose of paracetamol will be combined with glucuronide and sulphate before being excreted. Of the remaining 10%, about 5% will leave the body unchanged and the other 5% will be oxidized to benzoquinoneimine. The benzoquinoneimine is then combined with glutathione and becomes metabolised on to cysteine and mercapturate compounds before being safely excreted via the kidneys.

Because they have heard that a large dose of paracetamol can damage the liver, some people mistakenly believe that a small dose of paracetamol must therefore be able to cause minor damage to the liver. Taken long-term, in proper therapeutic doses, the liver and other organs should not be harmed by paracetamol.

If you take Oxycontin can you take Tylenol with codeine?

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Probably not, but maybe. You need to be tested in a doctor's office for such an allergy. You don't want to go into anaphylactic shock, so don't do any self testing!

What is the danger of taking 8 Tylenol ones at one time?

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It depends on the amount of acedeminiphon (sp) that is in it. Your daily maximum dose is 4,000 so you should be okay if it is 500/pill or less. But you don't want to make it a habit or else your liver or kindeys or both will give out on you.

How is Acetaminophen misused and abused?

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It can't be misused. just because it may be a "painkiller" doesn't mean it can be abused. it's tylenol, for god's sake. it will kill your liver. ten bucks says your some soccer mom thinking your son is doing drugs. he probably is.