vardenafil dosage information

Although rare, Viagra (sildenafil), Cialis (tadalafil) and Levitra (vardenafil) can cause muscle pain and unusual skin sensations or paresthesia. In clinical studies, Viagra caused muscle pain and paresthesia in less than 2% of patients. Patients who experience these side effects should stop taking the medication and consult their physician. These medications increase blood flow to the penis by inhibiting the enzyme phosphodiesterase type 5 (PDE5).

I’ve gone through a few articles mentioning that diabetics with ED can use Generic Levitra (vardenafil). Is that true? If so, I’d like to know who has used Generic Levitra having ED and diabetes and is it safe.

The PDE5 inhibitors sildenafil, vardenafil and tadalafil are competitive and reversible inhibitors of cGMP hydrolysis by the catalytic side of PDE5.

Thank you so much for the great information. The free's were not tested this time, but I will request that you are next time. Again, thank you.

Just looking for anymore information or advise about withdraws from Fioricet / I have been taking this medication from years from Migrain headaches, it's seemed the longer I was on it the less it helped so I would increase my doses because I could not get rid of my headaches the other day I just stopped using it because it was like just this non stop headache.

I drove two hours down to Louisville and spoke to a DR Cecil and he suggested that I try Infergen. Does anyone have any information about this drug. How is it taken, how often, what are the side effects? The Dr said that the effective rate is only about 20 % but I have few options left.

Thank you for sharing this info. I read your response on the other post as well. I hope that you do ok with the Neurontin. At least, with this dosage, you can build it up if necessary. I'm glad to hear that taking the pain meds. earlier helped out. Take care and feel better soon.

Hi everyone! As some of you know, I'm getting ready to start IVF in about a week and I'm currently taking 20 IU of lupron every night. They're switching me to 10 IU middle of next week and the 5 IU once I start the FSH meds. I'm a little worried about oversupression, but I can't seem to find much information online about what the most common dosage is. So here's my question....for those of you who have done IVF, what lupron dosage were you on?

i just discovered i have been giving my 41 year old daughter twice the amount of NEUTRA-PHOS-K powder as prescribed.....(the mgram amount is not listed on the packets) the prescribed dosage is one packet twice daily and i have been giving her 2 packets twice daily for about 2 weeks.....is she in any danger if i just go back to the prescribed dosage right now ?...

I have been taking 100mcg for years but now my doctor is changing my dosage to 88mcg. My tsh is .0005 and my t4 free is 7.56. Would those levels have caused hair thinning all over my body and hair texture change? My weight has pretty much stayed the same. I'm worried that the lowering of my synthroid will cause hairloss as my hair has just seemed to stablize recently. my doc thinks I have telogen effulvium due to stress in addition to the change in my thyroid.

I had the exact same problem of severe toe/foot/lower leg cramps that sometimes scared me. These started a couple of years after I started Synthroid. (The Synthroid saved me.) But my doctor should have told me what two of my friends told me who take Sythroid--that I needed to take Magnesium. Within a week or two the cramps were all gone, and my fatigue level was better. I'm SO THANKFUL! (I always take the Mag.

Although not as specific, it contain much of the same information and is readily available to the patient and the doctor. This information label was given to me by my GI to read and discuss regarding issues related to anger and depression and the potential for needing an AD sometime during trt. I would hope all doctors discuss this prior to trt, but this may not be the case. I'm also curious what "psychological evaluations" are being done.

As far as your erection problems and the penile length issues are concerned, you should start yourself on a 5 PDE (Phosphodiesterase type-5) inhibitor like sildenalfil or vardenafil under the care of urologist and see how you do. Once you have taken a trial of this drug, do get back to me and we can take it from there. Hope that this information helps and hope that you will get better soon.

If she has ketones we give her extra no carb fluids and contact per endocrinologist on how to adjust her insulin dosage. We do this because sometimes she has ketones due to being ill other times it is a missed bolus from the pump or not enough insulin. I would suggest you talk to your Childs endocrinologist or CDE on better ways for you as a team to get this situation under control. If they will not help you I would suggest you get a second opinion. For another pediatric endocrinologist.

Sorry, I don't have that information but I will provide it if and when I can get a hold of it. I was hoping for a general answer but I suspect it's a unique situation. I appreciate the quick response!

I just recieved my first prescription for methimazole, the directions is to take three 10mg daily. That seems to be a high dosage! I haven't taken any and will double check with Endo. Anyone else been prescribed 30mg daily?

thank you for that information. my husband and I were looking at the bloodwork and thought that the freet4 was a little high and wondering if I needed the decrease. now I know why I am feeling this way and I am not going nuts.

Since you have previous information posted, I suggest that you add this to prior thread so that all important information is in one place. Then you can request that this be deleted, since it would be a duplicate.

Thanks for your patience in answering my questions. That clarifies a great deal. This "old doc" of yours was the same one who wanted to reduce your dosage because you had mouth sores, I think it was, and he told you they wouldn't go away unless you stopped treatment..something like that, if I recall. I'm only going to tell you my opinion here. If I were in your shoes... I wouldn't dosage reduce with the information you've given.

If you are interested in trying this approach, I suggest you visit our Alternative Medicine Forum and talk to the folks over there. They are incredibly knowledgable and you will get excellent information from them. A word of caution............so many people think that if something is "natural," or "herbal," that it poses no risk and that can be a dangerous assumption. All pharmaceutical guides now list drug-herb-vitamin interactions.

Hey, Zpack works differently for different illnesses. Years of studies have shown the best treatment for chlamydia is 1g taken at once. That doesn't mean that a higher dosage won’t work, it’s just proven not to be as effective.

Although I am a big vitamin D supporter, the biggest problem with so much MS info in alternative medicine and various groups is that there are no double blind placebo controlled studies. With Ashton having a PH.D I am sure he is aware of that. Where are his "p" values???? Nothing he says or any of his other scientists for that matter can be proven to be statistically significant. There in lies the problem with the general population jumping onto these principles.

My doctor prescribed Flecainide (along with the Verapamil I was already taking) a couple weeks ago for what he diagnosed as atrial tachycardia. My holter report indicated more PAC's and PVC's than anything else. The Flecainide made my arrhythmias much worse, so I asked him to change meds. I'm now on Atenolol only and my symptoms are much, much better. I still have mild PAC's, but they are almost unnoticeable.

Take the insert out of the box and see if you Can make sense of the dosage information. Says you can start with a dosage of 100 mcg if you are under 50 years o,d or recently diagnosed with hypothyroidism. However if you are older than 50 or have cardiac problems you should start with .13 to .25. Therebis about 3 paragraphs of confusing dosage information.

you might just try eating one banana a day. That might help both your potassium levels and your hypoglycemia, as you say both are mild problems. And you might try supporting your adrenals with adaptogens such as eleuthero and ashwaganda. For exact potassium levels, that's hard, because potassium is a nutrient one has to be careful about -- you don't want too much, don't want too little. You might look into an electrolyte supplement -- and I don't mean Gator Aid!

Thyroid disease and what medication/dosage that works to alleviate symptoms is just as individual as you are. Barb's right when she said the healing takes time. I think you are doing the right thing, going up slowly and keeping track of how you feel, but try to relax a little, even though I know that's hard to do when you don't feel well. I wish I'd found this forum years ago, it's been very helpful.

Hi Scott and welcome, I'm very uncomfortable providing dosage information to anybody, it's never advisable on a public platform to trust accuracy of dosage information! I'm sorry but whilst you may have a legitimate reason for wanting to know, the potential for misuse of this type of information and the high complication risks with Rituximab (Rituxan) could result in very serious consequences....

Vardenafil dosage information

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