Alopecia symptoms and conditions

I WAS ON LOVENOX 1 SHOT PER DAY AFTER I WAS RELASED FROM THE HOSPITAL WITH SERIOUS DVT, LOVENOX KEPT ME OUT OF THE HOSPITAL.....BUT.....LOST 3/4 OF MY HAIR. IT WAS FALLING OUT IN CLUMPS, MY DR. SWORE UP AND DOWN THAT WAS NOT A SIDE EFFECT OF LOVENOX. FINALLY I GOT AN APPT. WITH A DERMATOLOGIST AND SURE ENOUGH HE TOLD ME THE ALOPECIA WAS A MAJOR SIDE EFFECT OF LOVENOX. I HAVE BEEN OFF IT FOR 6 MONTHS AND I AM GROWING MY HAIR BACK..FINALLY, BUT IT'S VERY SLOW GROWING.

I am also experience hair thinning while on Wellbutrin. I have had blood tests and there is no other detectable cause. The dermatologist said that she was only able to diagnose as possibly hereditary. However, I began noticing it shortly after starting 300mg of Well XL and then noticed increased thinning when I went up to 450mg. I don't take any other medications at all.

I searched the Wellbutrin prescribing information (a pdf on the official Wellbutrin website) and this is all I can find:

Other Events Observed During the Clinical Development and Postmarketing Experience of Buproprion

Adverse events for which frequencies are not provided occurred in clincial trials or postmarketing experience with bupropion. Only those adverse events not previously listed for sustained-release bupropion are included. The extent to which these events may be associated with Wellbutrin XL is unknown.

Skin: Rare was maculopauplar rash. Also observed were alopecia, angioedeme, exfoliative dermatitis and hirsutism.

----------------

Alopecia is hair loss. All that means is it was reported and they didn't do a study that would have produced data with which they could measure the likelihood that it is a Wellbutrin side effect. In other words, people said they were experiencing it but they can't confirm it.

I just dropped down to 300 mg and I'm contacting my shrink about tapering off completely - I feel like dealing with scalp showing through and feeling horribly self-conscious and unattractive because of it is not going to help my depression and self-esteem issues any.

I'm a woman by the way - the number of reports of hair thinning in women seems significant to me. I have no family history of thin hair on the female side that I know of.

I received my first shot of Gardasil in January 2007. It could have started sooner, but about a month later my hairdresser noticed a bald spot in the back of my head. I rushed back to my ObGyn and asked her if the Gardasil could be the cause as nothing else had recently changed. She said that she had not heard of this, but she referred me to a dermatologist. I asked him if my hair loss had anything to do with the Gardasil. He replied that I had Alopecia areata and one thing had nothing to do with the other. He advised that I continue with the Gardasil and that he would start treating me for the alopecia. I wish that I would not have listened. I don't know what would have happened if I had stopped then, but I didn't I proceeded with the treatment to the end now over half of my head is bald!!!
I don't know what to do. I keep going back to the dermatologist for treatments for the alopecia, but it just keeps getting worse.
If anyone has had a similar experience and would like to share or has found some other treatments that work, please post a reply.

Melissa

I received my first Gardasil shot on May 5, 2008 and about two days later I began to notice I was losing a lot of hair. I didn't fret because I had just gotten done taking finals and had been stressed to the max. I figured it was just my body responding to the stress. I have a lot of hair so it didn't phase me one bit. A week progressed and I would lose gobs of hair when I took out my hair band, brushed my hair, washed my hair, dried my hair. Now May 17, 2008, nearly 2 weeks later, my hair is half of what it used to be. I am freaking out. When I say I have lost alot of hair, I mean I can ball up the amount that comes out after a typical shower and it is about the size of a golf ball. I have not introduced anything new in my diet, nothing has changed, and I am not stressed. I am convinced this is due to Gardasil. Has anyone else experienced hair loss? If so, for how long? I am really scared.

After receiving my second vaccination I discovered pimples on my scalp, followed by hair loss. This condition is still reoccurring eight months later. Although doctors say this has nothing to do with Gardasil, it happened almost immediately after the second injection.

I've been on Advair for years. I'm a healthy 32 y.o female, active, with severe asthma. Trying to get myself off of it and have been successful at taking the medication once every 3 days or so. I am working out more and need it less often - the more I build up lung capacity. Within the last year, I've noticed that I've been losing eyebrow hair. So much of it, in fact, that I went to the Derm. for a diagnosis. They think it's "alopecia" - and I say ... it's ADVAIR. Anyone else experiencing hair loss or eyebrow loss, who happens to be on an inhaled steroid? In my case, it's only ONE eyebrow - very annoying! Hair on head is fine. Can't help but link it to the drugs, since Alopecia seems just way too far removed.

I just starting taking prednisone March/2/07 for alopecia. I havent had to many side effects so far, I take two dose a day at 20 mg. I do notice that I have a very hard time sleeping at night, one day I got off from work and cleaned up the whole house, couldn't stop cleaning. Of course I eat more, my face has gotten puffy within the last two weeks. I took this before 2 years ago and I had very bad mood swings on it, so I hope that doesnt happen again.

I have been taking Lisinopril for about the last maybe 8 to 10 years. It started with 20 miligrams and has now gone to 40 miligrams. Recently my pharmacy change the manufacturer of their Linsinopril. My face is extremely dry, as well as my hair has dried out so bad, that I am beginning to loose my hair. I honestly just received revelation of this on last night, as I could not figure out why I would stay so dry. I try to drink lots of water, but it seems that I am literally drying out. And to be honest my hair has had so many issues since being on this high dose of Lisinopril. Has anyone experienced dry skin or hair, resuluting in hair loss or extremely dry skin?

Hey all, I have posted several times on here. I am devastated about my tissue loss in my forehead. I am trying to pursue a lawsuit against a plastic surgeon in Michigan. My doctor tried to cover it up by immediately injecting me with a filler at MY COST and telling me it would last 5 years. Well guess what, 11 months later it disappeared and I got my medical records and found it it was cause she injected me with KENALOG 40! I only have one more year to file a complaint and so far this is hard. We really need to figure out a way to start a class-action lawsuit against bristol-Meyers-Squibb. Keep calling them, every little complaint helps!

These doctors could care less about us! I have had to be put on anti-depressants because my situation is right in the middle of my forehead. I am disfigured from a small procedure.

One surgeon I went to mentioned how hard it was to utilize Kenalog 40. It has to be diluted PRECISELY or else it will most definitely 'cause atrophy. This has to stop!!!!

I received Kenalog injections for alopecia. An associate in my dermatologist office thought it would be a good idea to increase the dosage so that i would get better results. Oh I forgot to mention the fact that I had hair all over my scalp. I just had some areas where the hair was thinner than other. However, I had no bald areas. Well that is until I was injected with a larger dose of Kenalog. I now have a dime size bald area in my scalp. The area is also hypopigmented as well. I mean white in color. Oh did I mention the fact that I am african american. So you can imagenine what it looks like. It has been 3 months. I still don't have hair the area and the area continues to be depigmented. I have consulted an attorney.

Has anyone noticed problems with alopecia with Lipitor? I have been on the medication for 5 years, and 2 years ago starting noticing thinning hair (female). I was off Lipitor for a few months recently, since I started back on the drug I've noticed I'm losing more hair again. I'm not experiencing the leg and back pain as others, but occasional swelling in the legs and feet.