I am taking tablets for my minor neural problem for the past 4 years, The tablets i am consuming are Oxcarbazepine (Trileptal) -300mg and Levetiracetam (keppra) -250mg. Now I am looking for a tablet which should have both of this content in the same. I feel guilty that I am taking more tablets and my health condition is improved now. so I planned to reduce my tablet dosage. so I look over this- i.e.
I see these color blobs that move in my vision that shouldn’t be there, they don’t show any connection to stimuli so I don’t have synesthesia. I’m on levetiracetam aka keppra and clobazam aka onfi. When I was on oxcarbazepine (trileptal) and levetiracetam (keppra) I started having these weird headaches where I would lose my vision, hearing, smell, and coordination, but I could still speak and feel. The doctors are pretty much stumped. Has anyone ever had a situation like this?
I am an Indian Citizen living in the US. I have been taking LEVETIRACETAM (to control partial-onset seizures) since 2011. Currently, I am in perfect health conditions. As a precautionary medicine, I get the medicine from India either myself or through a friend/family member traveling between India and the US. Due to the recent COVID-19 pandemic, I am running short of medicine. I have my prescription and medical certificates to support my condition.
can levetiracetam 750mg (2 2 times a day) be taken with amlodipine 10mg (1 time a day) and albuterol 90mcg (2 pumps 4 times a day). Can these be mixed? I this too much medicine?
At this point of time he is not able to speak more than two words in a row. His Hb is 8.9. He is on valporate, topiramate and levetiracetam. His MRI scan revealed "Assymetric Right Temporal Horn prominence without any difinite evidence of mesial scerosis"
His walking pattern is also erratic. Most often he adopts "Toe Walking". When he walks slowly, which is rare, he walks alright. Always he tries to rush up and runs in an imbalancing manner.
Hi there, the various side effects with keppra or levetiracetam are dizziness, irritability, tiredness, fatigue, severe allergic reactions, extreme dizziness, drowsiness, weakness or tiredness, memory loss, behavior changes like aggression, panic attacks, restlessness, new or worsening seizures etc. in the period immediately after a seizure attack, it could be the post ictal phase or confusion. Consult your neurologist for your evaluation and change of anti epileptic medication. Hope this helps.
As a general trend, all the anticonvulsant (anti-epileptic) drugs are used as treatment for bipolar disorder. Levetiracetam (Keppra) is no exception. At the same time, it is known to induce depression. It varies in different individual.
The lowest effective dose can be calculated at the dose of 20mg/kg.
Pharmacotherapy usually involves drug modulating GABAergic neurotransmission like Levetiracetam, Piracetam, Clonazepam or Valproic acid against prescription. I suggest you to consult neuro physician for his further evaluation and management. Take care and regards.
There have been reports of effective seizure control from patients following up monthly. They are using Levetiracetam (Keppra) as an adjuvant to another first line anti-epileptic medication. Most of them are suffering from partial seizures. And the first line drug is mostly Tegretol. Only a few patients have complained about mood swings so far. All had predominantly depressed mood, but not to the extent of being called depressive disorder. This must be about 10% of the patients.
carbamazepine, clobazam, lamotrigine, levetiracetam, oxcarbazepine and topiramate. These medications rarely stop the seizures completely but reduce the frequency and severity of them.
I hope this helps, my prayers are with you and your son.
Willy: Well, first let me say that I am mighty surprised and disappointed. I had expected that the same response dynamic would simply continue evenly across all genotypes.
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Why disappointed? Seems geno 2's fare better with Telaprevir than geno 1's and may be able to treat with monotherapy. As to geno 3's, it looks like only monotherapy didnt do well but maybe Im reading this study wrong.
SB 9200 is the Company’s novel small molecule nucleic acid hybrid (SMNH) compound being developed as both monotherapy and combination therapy for the treatment of Hepatitis B (HBV) and other viral diseases. The first portion of the ACHIEVE trial is a Phase 2a placebo-controlled, sequential-cohort, double-blind trial to evaluate increasing doses of SB 9200 as monotherapy for 12 weeks followed by tenofovir disoproxil fumarate (marketed by Gilead Sciences, Inc.
Pharmacological treatment when required would indicate anticonvulsants, like piracetam, levetiracetam, sodium valproate etc. 5-hydroxytryptophan can cause some improvement. Consult your neurologist. Hope this helps. Take care.
2X DAY, 10) METOCLOPRAMIDE 5MG. 4X DAY, 11) LEVETIRACETAM 1,000MG. 3X DAY, 12) DIVALPROEXE 1,000MG. 3X DAY, 13) VIMPAT 100MG. 2X DAY, 14) ZONISAMIDE 100MG. 3BEDTIME, 15) LANSOPRAZOLE 30MG. 2X DAY, 16) SUCRALFATE 1GM. 3X DAY, 17) COLESTIPOL 1GM. 3X DAY. I'VE TRIED VIAGRA BEFORE WITH NO RESULTS. I WAS ON WELLBUTRIN BEFORE ZIPRASIDONE. AT THAT TIME WHEN I HAD AN ORGASM I DIDN'T EJACTULATE ALTHOUGH NOW WHEN I AM ABLE TO ACHIEVE ORGASM I'VE GOT LITTLE EJACTULATION AT TIMES.
I have to ask: Was this your doctor's decision to treat you with monotherapy for this long ? Or did you push for it ? The reason I ask is I can't imagine what kind of logic the doctor employed to reach this decision to continue monotherapy for this length of time. I'm not ruling out an explanation that I haven't considered---there could be one in which case I'd really like to know what it was.
A phase II, randomized, double-blind, placebo-controlled study of nitazoxanide treatment for 24 weeks in 50 patients with chronic HCV-4 hepatitis was performed to evaluate the safety of prolonged administration and to determine the antiviral efficacy of nitazoxanide monotherapy (46).
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