Pizotifen :: Increased Sex Drive
Jun 5, 2009
I have only been taking 3mg for a couple of weeks, but the benefits are huge so far. I suffer from a continuous migrainous headache with regular migraine attacks, but atm I am totally headache free.
This past week I have noticed that my sex drive has increased, much to my husbands delight. I think this is probably because I am feeling so well and full of energy. But I also wonder if this is a possible side effect of the drug?
Has anyone else felt that Pizotifen has affected their sex drive?
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Any one else have increased sex drive?
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I just wanted to quickly share that since reducing from 100mg to 75mg, even in the short space of 3-4 weeks that I've already noticed a surge in my libido.
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I have had migraines since i was 12 (I'm almost 28 now) and over the years they have become increasingly frequent. It got to the stage where i was having 4-5 severe ones a week. I'm a medical student so this was REALLY getting in the way of life and i just used to wander round in a painkiller induced daze or be forced to collapse in bed.
A few weeks ago I came to the end of my tether. despite being on beta blockers and antidepressants and armed with seriously strong painkillers and all sorts of things like sumatriptan i was still completely incapacitated with a 4 day migraine. So i took the plunge and tried the pizotifen 1.5mg given by by GP.
Three days went by with no migraine... then a small migraine then another 4 day whopper probably more severe than before which knocked me out cold for the whole weekend and beyond. I've been on the pizotifen for 2 weeks now and low and behold today - another migraine.
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I am amazed and horrified to find that this drug is still being handed out to people with out proper supervision and advice. My husband was prescribed the drug a few years ago by his G.P. as his migraines had become more frequent, due to stress at work etc. He changed from someone who had little trouble getting up for work to a groggy, bleary eyed creature. Over the next 12 months he became increasingly belligerent, aggressive and unbearable to be around. He also experienced almost permanent numbness down his left side, like a mini stroke. I was just at the point of leaving this dark, brooding monster who was the antithesis of the funny, loving, intelligent man I married, when it occurred to me that this personality shift had taken place since he'd been taking this drug. Having picked one of his better moments to talk about this, he decided to stop taking the drug to see what happened. Within 24 hours my beloved husband was back. I got hold of the drugs and the information leaflet contained within it and realised that almost every side effect listed applied to my husband. Having been back to the G.P. together to discuss the effect this dreadful stuff had, she thought he should still take it and take anti-depressants as well, no thank you.
I had always suspected that many of his migraines were triggered by low blood sugar, no breakfast, missing lunch etc. and now he has adopted regular eating patterns in combination with the herbal remedy Feverfew he has only had two migraines in the last year. We were told subsequently by yet another G.P. at the practice that Pizotifen is only supposed to be prescribed for people with debilitating serotonin triggered migraines, that it is a drug of last resort for people who cannot function on a daily basis due to persistent attacks. He also pointed out that not only should it never been given to someone with the level and type of migraine he had, but also as he drives to work every day he should never have been prescribed this drug as it renders you unfit to drive or operate machinery, which the original G.P. should have known but never mentioned. . Thank goodness he didn't come to harm or cause any!!! We recently came across a couple pulling their hair out over their migraine suffering teenage son. He has recently been prescribed Pizotifen and has become so awful that they were considering throwing him out. We couldn't believe that it was happening to someone else and hence I searched out this site. It is a serotonin inhibitor. So unless you have migraines every day and you can't have any kind of life because of them find another treatment. Believe me when I say don't take this drug, not if you love your family.
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I was taking Sandomigrain for 10 plus years (0.5mg per day – I could not increase the dose as it made me too drowsy to function) and decided to slowly wean myself off as I was still having fairly regularly occurring Migraines that included visual and stomach symptoms. Over a period of a year I slowly cut down the 1/2 a tab in size and frequency till finally in December I was Sandomigran free. For the first 3 - 4 months everything was great, I had less migraines and headaches than I had ever had. Then in March, I woke up with an almighty pain in my head in the front half of my head. My blood pressure and pulse kept spontaneously elevating especially when I was asleep. This intense pain lasted for 2 weeks. Since then, I am left with a permanent Migraine which fluctuates in its severity and my brain (the front half) permanently feels as though it is in a contraction. I also have facial numbness and a sense of cold on my front and back periodically. After many tests (which have all come back clear) I am beginning to think that what is happening is a result of stopping the Sandomigran and of its consequential withdrawal. Has anybody else had these symptoms after stopping Sandomigran and if so, do the symptoms ever go away?
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I've just started taking the medicine and I'd like to know about any other drug without this side effect.
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I have been taking pizotifen for three months now, still no change. I get migraines everyday (3-4 episodes), and gaining weight by the second. I'm taking Maxalt (Rizatriptan), but nothing seems to make them go away. I have an MRI scan next month....
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I've been on Propranolol 80mg for my migraines which have worked very well. One issue with them is that I can wake up during the night and I have great difficulty in getting back to sleep. This results in me being quite tired during the day, as I drive 45mins to get to the office and sometimes 4-5 hours if I'm on site then it was a concern.
I saw the doctor on Friday and he suggested trying Pizotifen, he told me they can cause drowsiness but if I take it at night then I should be OK by the morning.
I've been reading through the experiences here and I'm not too sure about taking them now, I haven't been to the pharmacy with the prescription and I'm unsure whether to bother.
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I was tapering off clozapine and my paranoia came back. I went from 300 to 250 in a week then from 250 to 200 in another week and so on until I got down to 50. When my paranoia came back, I immediately started taking 200. Should I have slowly increased my dose? After I increased it, I got a sore throat for three days and a runny nose with lots of coughing up phlegm for a week. I'm wondering if it's from the clozapine. Is it dangerous to increase clozapine like this?
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A recent study showed 20 years on most patients' Barrett's segment lengths remained the same as at initial diagnosis.
Thus it was with some confidence I approached my surveillance gastroscopy yesterday that my 3 cm circumferential band of non-dysplastic Barrett's would show no changes.
Awake throughout the rather longer than usual procedure (unfortunately sedation has no effect on me), I listened to the doctor call out the distances to her recording nurse as she took 20 biopsies and realised this was longer than 3 cm.
"8 centimeters", she confirmed when I asked her afterwards. ""Full circumference lower down and patchy higher up."
I was astounded. With my Nissen fundoplication years ago and the Collis-Nissen revision last year reducing reflux, I hadn't expected that.
It took my wife to unravel the blindingly obvious.
"Doesn't the Collis procedure lengthen your oesophagus?"
"Yes."
"And what constitutes that increased length?"
Of course. The extended oesophagus is lined with gastric cells. And the length of that extension? - About 5 cm.
The biopsies for the bottom 5 cm will show gastric cells which, depending on histopathology, may be interpreted as gastric metaplasia but not intestinal metaplasia.
I feel sure my previous 3 cm of non-dysplastic Barrett's remains unchanged but has 5 cm of stomach cells lining the extended oesophagus below.
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I just got my results and it says that I have increased protein in urine? What are the possible causes of high levels of protein in urine? I would like some explanation.
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My psa level increased from 4.2 at the end of 2012 to 6.6 twelve months later at the end of 2013. My doctor sent me to a urologist who ordered another psa test and that came back at 11.00. There was only 3 weeks between my 6.6 reading and this latest one at 11.00. The urologist thinks that this huge increase is unlikely to be a cancer and wants me to have another test in 4 weeks time.
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I'm on day 3 of 40 mg (I did two weeks on 20 first) Day one I was okay but yesterday I felt completely scattered, anxious and couldn't keep it together. I've just (sort of reluctantly) taken my dose today, day 3. I've read that the first week of an increase can be rough. Any advice? I've been on lexapro previously for depression and anxiety but my current doctor thinks that I have ocpd (which leads to my dep/anx) so she is trying the fluoxetine. I really really want to be able to function better.
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I took my first dose of 6 - 2.5mg pills last night for my arthritis. Woke up a few hours later in the most excruciating joint pain I have ever had--in EVERY joint including my knuckles of my fingers. Anyone ever experience this crazy reaction to this medication?
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I am a 38 year old male that has been experiencing some problems lately. I find myself fatigued from morning til night, around the clock. I have no motivation or energy to do ANYTHING. It's beginning to affect my work life as well as my sex life. I literally have no sex drive and I am engaged to the most wonderful woman. However I am so scared to lose her and feel as though she thinks I don't desire her.
I have had to sets of blood work done to see what's going on. Results came back showing my testosterone was low. A lot of the numbers and data I have no Idea what it means. However when he said the normal testosterone range for males was mid 300-s up to 1100 and mine came in at 241...I obviously am very concerned.
He sent me to an endocrinologist to have even more work done so that they could determine treatment. Needless to say, I'm nervous, exhausted and feel like I'm existing away.
I will admit, I didn't do my body good in my early 20's as I did take steroids to bulk up. It have me energy and I felt great. But did I ruin my body? It's also hard to say...because maybe I have low T back then and the steroids helped me feel better!? Idk. I would like to have energy again, a sex drive, and have kids with my beautiful fiance one day.
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I've been on Mirtazapine (30mg) for roughly 10-11 months now after suffering with my second bout of severe depression in 2 years and although this drug has helped me overcome my depression, I cannot seem to get rid of the excess weight that I have gained whilst taking it.
I am a very active guy, I play football twice a week and do lots of cardio but it seems whatever I eat, it goes straight to my belly. This has pretty much always been the case with me throughout my life.
I think I was roughly 15.5 stone when I started on Mirtazapine in July 2014 but I now weigh roughly 17.5 stone. I am 6ft7 in height so I guess I needed to put on a few pounds (as I was quite slim previously) but 2 stone is a rather big weight gain.
For an unknown reason I always feel hungriest late at night, does anyone else get this symptom? I take the tablet every night before I go to sleep (around 10:30pm).
How long are you supposed to take this drug for before reducing the dosage? Obviously the last thing I want is to become depressed again so I don't mind taking it but I would be interested to see if my weight decreases if I was to lower the dosage to say 15mg.
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I've recently upped my dosage of paroxetine to 30 mg following the doctor's advice. I'm on day 6 of 30 mg and wondered how long it would take for me to get back to "normal". I was in 20mg but it suddenly stopped working 3 1/2 months ago and I had a suicidal episode. Since then I have been living in fear and am constantly in edge. I am a single mum to a 16m girl and I just want to get back to normal and be a good mum. Please help if anyone has any experience of upping their dosage!
I am scared of being on my own in case I have another episode like the one 3 months ago where I had to be taken to hospital. It was very traumatic and has ruined my life. I know I don't want to kill myself, I wouldn't do that to my daughter or family, I just get strong waves sometimes and feel exceptionally low. I know this has occurred because of a mess up of my medication, when weaning me off the tablets, the doctor I'll advised me to cut them in half. I now know this was a stupid thing to do. I just wondered how long it will take me to even out or if I'm ever going to get back to " normal"
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I stopped smoking weed 8 days ago, i'm 53 and i've smoked it from being a teenager, very light smoker, 1 or 2 small single skin spliffs a night, but not every night, i'm experiencing anxiety mainly due to sound, sounds seem magnified! my partner may put her knife and fork down after eating and i nearly jump out of my skin, its not good.... i play in a band and iv always seen it as part of being a musician, playing loud music is ok its these random small noises that are grating on my nerves.. anybody else experienced this?
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I have been on 20mg Citalopram for years. Although lately I feel this has not been working as I have felt low, tearful,tired,unmotivated and generally not right. I have not been going to work and used to love my job even having to do 12hr shifts. I have been sick alot and suffer back and joint pains and being investigated for Rheumatoid Arthritis or some other autoimmune problem. My main concern is my mood ad I just want to be normal and go to work and socialize again. How long does it take to see an improvement it's been a week since dose change? Sorry for long post just had to get how I feel out there.
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I've never had vaginal odor before... And now that I'm pregnant I have increased discharge and vaginal odor. I've been using feminine wash but nothing seems to help.... ?
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