Review: could Acyclovir cause Substance abuse (Drug abuse)?
Summary: there is no Substance abuse reported by people who take Acyclovir yet.
We study 552 people who have side effects while taking Acyclovir from FDA and social media. Find out below who they are, when they have Substance abuse and more.
You are not alone: join a mobile support group for people who take Acyclovir and have Substance abuse >>>
Acyclovir has active ingredients of acyclovir. It is often used in herpes simplex. (latest outcomes from 1,292 Acyclovir users)
Substance abuse has been reported by people with drug abuse and dependence, pain, depression, back pain, stress and anxiety. (latest reports from 10,556 Substance abuse patients)
On Jan, 30, 2015: No report is found
Do you have Substance Abuse while taking Acyclovir?
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- Anyone else experiencing these rare & unbearable side effects from shingles treatment?
The very day I start treatment I can't stop needing to urinate, can't sleep, and get very shaky and/or have tremors. My BUN/Creatinine levels only become abnormal immediately after I start taking the medication. Nothing helps the insomnia or restlessness.
I've had an active Shingles infection for over a year (maybe much longer). I was born infected to Chicken Pox (which included related birth defects such as Bell's Palsy) along with a severe defect in a protein gene that makes up my primary immune system. Is anyone else experiencing this???????????????????????? If so please get in touch with me. Thank you.
- Shingles is a terrible experience
Wednesday: broke out under arm and on left back. Severe Sharp stabbing pin under arm and thru left breast. Had just had a small cancer removed from right ear and pain was similar, so I thought it might be a cancer so
Friday: went to doctor was told it was Shingles was given Acyclovir. Told to us Calamine lotion on the lesions. Calamine did nothing for the itching. Went on Internet and read everything about Shingles. Started using Coconut Oil.
Saturday: pain was terrible. Applied the coconut oil.
Sunday: Went to Health Food Store and purchased Licorice Tincture, Olive Leaf Tincture, l-Lysine, Colloidal Silver gel and Vitamin B-12 sub-lingual tablets. The Licorice made it feel better for a little bit. Colloidal Silver helped. The Olive Leaf Tincture really worked with the colloidal Silver. Actually gave the most relief. My husband had knee surgery 3 years ago and had been given a circulating ice water machine. Several sites had recommended using a cold cloth on the lesions, so I put the circulating ice water blanket on my back. It really gave me relief. For about 3 days, it circulated on my back, while using the Olive Leaf and Silver.
Wednesday, it's been 7 days and my lesions have scabs on them and are getting less red every day.
Something else that I have done is stand in the shower and let hot water run on my back. This has been very soothing.
Thursday: Was reading about Bicarbonate of Soda curing cancer and knowing that this would make the body alkaline, and nothing lives in an alkaline environment, I started drinking water with soda in it. Will be curious to see if it attacks the Shingles. One of the things recommended was using Soda on the Shingles, so attacking it from the inside should work better.
- Ideopathic hypersomnia from mantle cell lymphoma
I have an unusual idiopathic hypersomnia surrounded by the circumstance of also having Mantle Cell Lymphoma. I awake each day at around 7:00 am without an alarm after 7-8 hrs sleep. By 8:00 am after a cup of coffee and breakfast, I feel fully awake and 100% normal.
Around Noon and 12:30, I begin to feel sleepiness coming on. This is nothing like the mid-afternoon low many people experience. A cup of coffee or a little fresh air do nothing.
By 1:00 pm - 1:30 pm, I feel deeply drugged (like I've taken Ambien) and need to sleep. I sleep 3-4 hours of fairly deep sleep (I don't hear the phone or someone at the door). I have vivid dreams near the end of the nap and about half the time I have auditory hallucinations at the beginning or the end of the nap (I generally don't have these at night).
When I awake, I feel like it's morning again and need a cup of coffee to get me going again. For the rest of the evening, I feel about 80% of morning alertness and energy levels.
I go to bed at about 10:30 every night. It takes me about 15 - 20 minutes or so to fall asleep. I get up once a night to urinate, due to slight incontinence from prostate brachytherapy. I generally fall right back to sleep. Even when I sleep more or less than average, or go to bed significantly later than normal, I still feel the 1pm sleepiness at the same time and in the same duration.
I have tried Nuvigil and it works well enough for me to stay awake during the afternoon if absolutely necessary. I'm feel about 70% of normal, but don't sleep well that night and don't feel fully rested or awake the next day. If I force myself to stay awake, the intense sleepiness goes away around 4:00pm - I feel sluggish but do not need to sleep until my normal bedtime.
Diagnosed with Mantle Cell Lymphoma in June of 2013. I noticed worsening early afternoon sleepiness up to six months before diagnosis. After diagnosis, I gradually became more sleepy and began needing naps of 1/2 hour to 1 hour. By the time I began treatment for MCL (Oct 2012, I was sleeping in excess of 4 hours every day despite getting a good night's sleep. This and the increasing size of my spleen were the determining factors for beginning treatment. During 6 months of chemotherapy (Rituxan/Bendamustine every 4 weeks) I continued to have these naps. After achieving full remission, I received high dose chemo followed by an autologous stem cell transplant in May of 2013. About a month after the transplant, when I gained a little strength back, I needed only a light nap of 30-45 minutes, but gradually the heavy naps returned to the current 3 hr/day level, despite my strength and endurance returning to nearly normal levels. My nighttime sleep pattern has not changed significantly all this time.
I had an Overnight sleep study that showed no significant apnea, but because I didn't sleep normally at the center, the test was inconclusive. It was followed by an MSLT which showed that I did not have narcolepsy (no early REM). I was then prescribed an auto-PAP machine for three weeks to check my sleep hygeine at home. Minimal apnea was noticed, and most of the episodes were from my changing position triggering a boost in the PAP pressure. I slept significantly worse because of this.
Because of the clockwork nature of the daytime sleepiness and the correspondence with my lymphoma, I would like to investigate an endocrinological source for my idiopathic hypersomnia but the sleep centers here in Wilmington are not equipped to handle this investigation.
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