Sunday, July 31, 2011

savella update.

i'm alive!


so so sorry i've been gone. i'm trying to get used to the new savella and develop a routine with it.


here's a little more information on the savella (taken from webMD):



This medication is a serotonin-norepinephrine reuptake inhibitor (SNRI) that works by helping to restore the balance of certain natural substances in the brain(neurotransmitters).
Dosage is based on your medical condition and response to treatment.
To reduce your risk of side effects, your doctor may start you at a low dose and gradually increase your dose. Follow your doctor's instructions carefully. Do not increase your dose or take this medication more often than prescribed. Your condition will not improve any faster, and the risk of serious side effects may be increased.
If this medication has been used regularly for a long time, withdrawal symptoms (such as mood swings, headache, tiredness, sleep changes, and brief feelings similar to electric shock) may occur if you suddenly stop using this medication. To prevent withdrawal reactions, your doctor may reduce your dose gradually. Consult your doctor or pharmacist for more details, and report any withdrawal reactions immediately.
Nausea, vomiting, dry mouth, constipation, loss of appetite, dizziness, increased sweating, headache, or hot flashes (flushing) may occur. If any of these effects persist or worsen, tell your doctor promptly.
Remember that your doctor has prescribed this medication because he or she has judged that the benefit to you is greater than the risk of side effects. Many people using this medication do not have serious side effects.
Tell your doctor immediately if any of these unlikely but serious side effects occur: fast/pounding heartbeat, changes in sexual ability, decreased interest in sex, painful/difficult urination.
so i've bolded the issues i've experienced while taking savella. it's only been ten days; the last three days, i've been taking the 50mg dosage. i wake up in the morning and take it before 6am, then between 7:30-8:30 right before i get ready for bed. it helps me fall asleep a bit.
i tend to get really scatter-brained and foggy, especially at work, since that's where i am for the greater part of the day. and the nausea?! it's ridiculous sometimes! and i get extremely exhausted. i honestly do believe it's the medication. but i'd rather experience that than the pain of fibromyalgia. since taking it, i've been able to take every day as it comes. i was actually able to enjoy my vacation! i'll save that for the next post...

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