Grab his tail
Gila Venom:
Their venom comes from glands within the lower jaw, and flows into a bite through channel in grooved lower teeth. Although the toxin is as toxic as that of a diamondback rattlesnake, this simple delivery system introduces the toxin into a wound fairly slowly. The effect of the bite may be intensified as the animal clamps down next to his jaws and rolls over, hanging onto its sufferer and continuing to bite and chew as the venom accumulate in the wound.The toxin attacks the nervous system and is strong plenty to kill birds and mammals. It have been suggested that the toxin of the Gila monster is used more for defense than for feeding.
The bite is described as extremely raw, although pain is initially confined to the nouns of the bite. Victims may also experience localized swelling, nausea, vomiting, hypertension, weakness, wooziness, excessive perspiration, chills, and fever. When bitten, it is esteemed to disengage the lizard as soon as possible. This may be done by placing a strong stick between the bitten part and the wager on of the lizard's mouth and pushing against the rear of the mouth. If this doesn't work, immersion in river may make it release its hold. The brittle teeth of the Gila monster may remain imbedded surrounded by the wound and must be removed by a medical professional.
Wednesday, November 30, 2011
how do you receive a perscription card to fashion buying MJ permissible?
It really depends on where you live. About 7 years ago, you could see a Physician at the "Cannabis Club" surrounded by Arcata, CA for the walk-in fee of 250 bucks. You after gave a rationale for your need for this perscription (cataracts, help your appetite, helps you combat heroin addiction, etc.) and you were issued a card. This also allows you to purchase the medical-grade cannabis. :)
First of adjectives what is MJ?
i dont kno.
You might get it from the doctor as a twinge killer. Didn't you ever see that Simpsons episode where on earth Homer got medical marijuanna?
Come on, don't catch the Rx card unless you really *need* the drug therapy. It's wankers who ill-treat the system that make medicinal marijuana look unpromising to the policymakers and the rest of society. There are folks who have legit involve for drugs. If you are not one of them, it's not fair to nick advantage. Abusing the system results within the recriminalization of pot for everybody.
First of adjectives what is MJ?
i dont kno.
You might get it from the doctor as a twinge killer. Didn't you ever see that Simpsons episode where on earth Homer got medical marijuanna?
Come on, don't catch the Rx card unless you really *need* the drug therapy. It's wankers who ill-treat the system that make medicinal marijuana look unpromising to the policymakers and the rest of society. There are folks who have legit involve for drugs. If you are not one of them, it's not fair to nick advantage. Abusing the system results within the recriminalization of pot for everybody.
How do you find out what is the concentration of the solution?
two methods
(1) by titrimetric method: in this method, concentration of the solution is determined quantitatively by react or titrating equivalent amount of compound (which is to be determined and have unknown concentration) near another compound of known concentration and particular volume.
N1 . V1 = N2. V2
N1 = (N2 . V2)/V1
N1 = normality of compound of unknown concentration.
V1 = volume of compound of unknown concentration consumed during titration or reaction.
N2 = normality of compound of particular concentration.
V2 = volume of compound of known concentration consumed during titration or spontaneous effect.
(2) spectrometric method:
in this method two solution is prepared: first is the tryout solution which contain compound of unknown concentration and second is the standard solution which contains same compound of known concentration. graph is obtain and by comparing graph and their extinction coffecient, concentration of compound of unknown concentration can be determined.
for detail see A. I. Vogel's textbook of quantitative chemical analysis.
2 ways
1) Assuming it is visible by some from of spectrometry, net several known concs of equal soln. Draw a graph (stnd curve ) plooting these points. Measure the unknown, and read on the graph what concentration your spectrophotometric reading relates to.
2) send it down a mass spec and determine how much is surrounded by your original example (quicker and easier IF you have a mass spec and you know how to use it!)
titration next to a known solution im guessing
(1) by titrimetric method: in this method, concentration of the solution is determined quantitatively by react or titrating equivalent amount of compound (which is to be determined and have unknown concentration) near another compound of known concentration and particular volume.
N1 . V1 = N2. V2
N1 = (N2 . V2)/V1
N1 = normality of compound of unknown concentration.
V1 = volume of compound of unknown concentration consumed during titration or reaction.
N2 = normality of compound of particular concentration.
V2 = volume of compound of known concentration consumed during titration or spontaneous effect.
(2) spectrometric method:
in this method two solution is prepared: first is the tryout solution which contain compound of unknown concentration and second is the standard solution which contains same compound of known concentration. graph is obtain and by comparing graph and their extinction coffecient, concentration of compound of unknown concentration can be determined.
for detail see A. I. Vogel's textbook of quantitative chemical analysis.
2 ways
1) Assuming it is visible by some from of spectrometry, net several known concs of equal soln. Draw a graph (stnd curve ) plooting these points. Measure the unknown, and read on the graph what concentration your spectrophotometric reading relates to.
2) send it down a mass spec and determine how much is surrounded by your original example (quicker and easier IF you have a mass spec and you know how to use it!)
titration next to a known solution im guessing
how do you numeral micrograms per minute?
It kind of depends on what you are starting near but lets say aloud that you have a solution of drug containing a concentration of 20 milligrams per milliliter and you are running it at 2 milliliters per hour. You inevitability to multiply it out to convert the units. If you are starting next to 20 mg/mL at 2 mL/hour, first you convert hours to minutes and then you convert mg to micrograms. The mL dissolve, the mg cancel, the hours quash, and the units you are not here with are micrograms per minute!
__20 mg___ x __2 mL___ x ___1 hour___ x _1000 mcg__ =
1 mL 1 hour 60 minutes 1 mg
There are other ways to do it, but I find this the easiest. If you necessitate to figure out mcg/kg/minute, you merely divide the last number by the patient's counterbalance.
of what? thats too vague, you own to give much more detail. the prefix micro- scheme millionth, a microgram is a millionth of a gram.
ah well no model
Divide mass by time and convert.
__20 mg___ x __2 mL___ x ___1 hour___ x _1000 mcg__ =
1 mL 1 hour 60 minutes 1 mg
There are other ways to do it, but I find this the easiest. If you necessitate to figure out mcg/kg/minute, you merely divide the last number by the patient's counterbalance.
of what? thats too vague, you own to give much more detail. the prefix micro- scheme millionth, a microgram is a millionth of a gram.
ah well no model
Divide mass by time and convert.
How do you get the impression just about the D.H.S. announcement that they are lifting the moratorium on drugs bought from Canada
2) Why is the D.H.S. involved in this? I know the Customs issue, but how am I threatened by gramps ordering his Viagra from Canada?
Also, next to more people buying more drugs from countries bar the U.S., how do you feel that will affect prescription prices here? Being from Canada, I own mixed feelings. One of the reason drug prices are lower here are the government controls on pricing. Why should other countries benefit from our rates money? Get off your butts and go beyond some similar laws within your own country.
On the other hand, I am against exploitation of people's suffering by the sizeable pharma corporations, even though I own stock in a couple of them.
As far as why the DHS desires to be involved, I guess it would be because there is some concern that Canadian drugs are not quality-controlled to U.S. specifications, and they are worried almost fake drugs cause harm to ethnic group. What if Gramps takes some bogus Viagra that make him go postal and comes to your conservatory and goes on a rampage next to his hunting rifle etc etc.
LAWYERS and liberals caused this problem,
endlesss canon suits and endless whining equals
COLD HARD CASH BABY!
Also, next to more people buying more drugs from countries bar the U.S., how do you feel that will affect prescription prices here? Being from Canada, I own mixed feelings. One of the reason drug prices are lower here are the government controls on pricing. Why should other countries benefit from our rates money? Get off your butts and go beyond some similar laws within your own country.
On the other hand, I am against exploitation of people's suffering by the sizeable pharma corporations, even though I own stock in a couple of them.
As far as why the DHS desires to be involved, I guess it would be because there is some concern that Canadian drugs are not quality-controlled to U.S. specifications, and they are worried almost fake drugs cause harm to ethnic group. What if Gramps takes some bogus Viagra that make him go postal and comes to your conservatory and goes on a rampage next to his hunting rifle etc etc.
LAWYERS and liberals caused this problem,
endlesss canon suits and endless whining equals
COLD HARD CASH BABY!
how do you evaluate the dermal toxicity of modern drug?
During preclinical tox testing, mice are the most adjectives.
According to the FDA guidance on woundcare products (from the CDER website):
When preclinical studies or previous clinical experience suggest that a topical product might induce clinically significant dermatitis, irritancy or sensitivity testing surrounded by normal volunteers is recommended prior to trials contained by patients, since superimposed dermatitis is deleterious to wounds. The need for routine conducting tests of the final formulation depends on the product, and sponsors are encouraged to discuss dermal toxicity trialling with the appropriate Center up to that time initiating the studies.
Here is an exapmple of a Percutaneous Absorption Study for a topical drug product..
Toxicity/Irritation Tests:
Acute Toxicity (LDn)
14-Day Dermal Toxicity and Irritation in Mice
7-Day Dermal Irritation within Guinea Pigs
Primary Skin Irritation in Guinea Pigs
Primary Eye Irritation contained by Rabbits
13-Week Dermal Toxicity and Irritation Test in Rabbits
91-Day Dermal Irritation and Toxicity Study
rub it on your skin :) sorry, bleak joke.
According to the FDA guidance on woundcare products (from the CDER website):
When preclinical studies or previous clinical experience suggest that a topical product might induce clinically significant dermatitis, irritancy or sensitivity testing surrounded by normal volunteers is recommended prior to trials contained by patients, since superimposed dermatitis is deleterious to wounds. The need for routine conducting tests of the final formulation depends on the product, and sponsors are encouraged to discuss dermal toxicity trialling with the appropriate Center up to that time initiating the studies.
Here is an exapmple of a Percutaneous Absorption Study for a topical drug product..
Toxicity/Irritation Tests:
Acute Toxicity (LDn)
14-Day Dermal Toxicity and Irritation in Mice
7-Day Dermal Irritation within Guinea Pigs
Primary Skin Irritation in Guinea Pigs
Primary Eye Irritation contained by Rabbits
13-Week Dermal Toxicity and Irritation Test in Rabbits
91-Day Dermal Irritation and Toxicity Study
rub it on your skin :) sorry, bleak joke.
how do you die from cancer?
I know cancer might be deadly but why do you die? Is it because a body can't survive beside less than a ceirtain number of cell (after a bunch has be attacked) or is it because of a kind of some gentle of poisoning? my dad died of lung cancer. The cancerous cells replaced the worthy ones and didnt do the job of the feeble ones. Cancer kills because the organs artificial stop working as their working cells are replaced.
Cancer cell gobble down everything, including fellow cells. So, as the disease progresses, the body is both starved of nutrients, and the incapacitate becomes too much to repair.
One of the frightening things around cancer is the possibility of metastasis. This is the process where millions of malignant cell are released from the tumor (the primary) into the bloodstream. Fortunately, most of these cells are kill by trauma produced while traveling within the blood vessel walls, or by circulating cell from the immune system, like the Natural Killer (NK) cell and other T lymphocytes. Other immune cells that fight malignant cells are macrophages, antigen-presenting cell, and substances produced by immune cells call lymphokines. One common lymphokine is call interleukin-2 (IL-2) or interferon. (See How the Immune System Works for details on these different components of the immune system.) In some cases, the circulating malignant cells survive and fit tightly to the inner muscular lining of the blood vessel walls. Here the process of tumor formation can instigate in a different nouns of the body (the secondary), causing further destruction.
Cancer cell gobble down everything, including fellow cells. So, as the disease progresses, the body is both starved of nutrients, and the incapacitate becomes too much to repair.
One of the frightening things around cancer is the possibility of metastasis. This is the process where millions of malignant cell are released from the tumor (the primary) into the bloodstream. Fortunately, most of these cells are kill by trauma produced while traveling within the blood vessel walls, or by circulating cell from the immune system, like the Natural Killer (NK) cell and other T lymphocytes. Other immune cells that fight malignant cells are macrophages, antigen-presenting cell, and substances produced by immune cells call lymphokines. One common lymphokine is call interleukin-2 (IL-2) or interferon. (See How the Immune System Works for details on these different components of the immune system.) In some cases, the circulating malignant cells survive and fit tightly to the inner muscular lining of the blood vessel walls. Here the process of tumor formation can instigate in a different nouns of the body (the secondary), causing further destruction.
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