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I’m terrified.
After my suicide try and subsequent psychiatric hospitalization in 2014, all my remedy was modified. I used to be began on a special antidepressant (Pristiq, 100 mg.) and a special antipsychotic (Abilify, 15 mg). In 2018, following my stroke I turned severely depressed and returned to remedy. My therapist, Dr. Lev, added a second antidepressant (Remeron, 45 mg.) to my cocktail. I’ve been secure on these drugs ever since.
I began a brand new job this yr. Which means new insurance coverage. Once I ran out of the Pristiq, Dr. Lev needed to ship in a refill to the pharmacy which triggered a previous authorization request from my new insurance coverage firm. Sadly, by the point she obtained notified that prior authorization was vital, I solely had one pill left, which I took this morning.
In an article printed by the AMA, Jack Resneck, a dermatologist and instant previous president of the AMA, writes about prior authorizations, “A few years in the past, medical health insurance plans got here up with this course of, and on the time it was only for brand-new, costly drugs that had simply come to the market or new remedies that they needed to restrict use of.”
I can handle one or two days with out the Pristiq, however greater than that I begin to fear. I’m anxious that I’ll begin to undergo withdrawal or what’s extra formally known as antidepressant discontinuation syndrome which may occur should you cease taking your remedy abruptly.
In accordance with The Cleveland Clinic, “Antidepressant discontinuation syndrome (ADS) can occur should you cease taking your antidepressant should you’ve taken it for at the least six weeks. It’s extra prone to occur should you abruptly cease taking the remedy as an alternative of slowly petering out below the steering of your healthcare supplier.” Moreover, “ADS causes a number of signs, together with insomnia, nausea, and flu-like signs.”
ADS sounds crummy, however it’s one thing that may be endured. What I’m actually frightened about is: What if the insurance coverage firm denies the Pristiq, or denies the 100 mg. dosage, citing that fifty mg. is the utmost?
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Resnick’s AMA article states: “As we have a look at what issues require prior auth … it used to actually be a slim set of brand-new issues that had simply come out, however now it is fully unpredictable.”
I fantasize about Dr. Lev, within the peer-to-peer overview with an insurance coverage firm rep on the opposite finish of the telephone, or nevertheless they do it today, telling this individual, who might or might not be a psychiatrist, that this affected person has a historical past of extreme psychotic melancholy, that she has tried suicide 4 instances, that she has been secure of the 100 mg of Pristiq for 10 years.
She is going to inform them that there’s a probability that if she is denied the 100 mg. of Pristiq, she’s going to grow to be so severely depressed that her suicidal ideation will return. And she’s going to quote a examine printed in The American Journal of Psychiatry and inform them “A previous historical past of suicide try is taken into account one of the crucial sturdy predictors of ultimately accomplished suicide.”
Will I matter to them?
