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Just wanted to let everyone in the U.S. know that if you want the cheapest price on Eucrisa, you should call them directly to get the best copay savings card. They're at 1-833-956-DERM.
There is more than one savings card. The one you sign up for online only reduces your cost to a minimum of $100 in some situations, for instance. But I called them directly, and now the cost is $35.
You have to get the pharmacy to run the BIN and other numbers from the savings card they email you after you talk to them on the phone.
Here's the website with the phone number, but again don't get the savings card online, call them directly: EUCRISA® (crisaborole) & Pfizer Dermatology Patient Access
Just thought I'd share this since I've spent an hour on the phone (going back and forth with the pharmacist and Pfizer and getting all the deets). And don't let the pharmacist tell you "oh, all the cards only reduce it to $100," since I just called back and made them actually run my specific card as secondary insurance with the BIN number, and now it's $35.
If your insurance covers any part of Eucrisa, I think you can get it even cheaper if you call.
If you have government insurance like Medicare or Medicaid, or if you're uninsured, there is a separate program for you at that number. A few years ago when I was uninsured, I got it for free.
Eucrisa helps me so much with my facial eczema, so I thought I'd spread this info since it's not apparent on the site.

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Therefore witchcraft or love spells should not be the ultimate solution to mending a broken heart in a relationship, one has to make love exist naturally by doing the right things to your partner, the things that will recapture the inner feelings of love and affection as you did in the start of the relationship.
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Okay so I know that asking it through the phone or texting is suspicious but then they're offering it also through the email portal but I'm not really sure what the thing since they also offer it over phone with voice and phone over text which I find very sus.
And in case you're wondering no, it's not emergency services or anything like that. I'm not dying, I just need to set up an appointment.
I'm just trying to figure out which one I want and this one is like,
We need your insurance information, so I give it, and then they say that they need a bunch of information like my name, my birthday, and stuff like that, and then they say they want my credit card information and then I'm finding that really weird and then they send me an email and there I can log in and then put my credit card information into that but I'm still very nervous and I'm worried they're going to give me a co-pay and I can't afford a copay.
I live in US by the way.

Hi folks, wondering how people are phoning multiple pharmacies and then racing to one with supply, to get their prescription filled. My prescription is currently with CVS so I know all CVSes can fill it but how would I suddenly rock up at a non CVS pharmacy and request Zepbound? I read it can take several days for a prescription to transfer between pharmacies.
For reference, I’ve just been prescribed Zepbound and haven’t managed to get my first prescription filled yet. Thanks!

I switched from Adderall XR to Vyvanse hoping it won’t have the same side effects, or at least not the same degree.
My insurance has the copay for Vyvanse $375! It’s also been tough getting the generic since the shortage is still going on and pharmacies in my area can’t get it.
I’m hoping that switching to an online pharmacy might help, I have my fingers crossed.
What should I do?

My doctor is requiring me to pay my copay of $40 + 3% surcharge to secure my appointment on Thursday. I live in Texas and I’ve never had this happen to me before.
Is it legal/normal to charge a 3% fee for paying with a credit/debit card (even with FSA)?
Here’s the text message I received:
[PATIENT], the amount due for your appointment is $40 +3% surcharge =$41.20. IN ORDER TO SECURE YOUR APPOINTMENT, please kindly make the payment one day/24 hours before your appointment to avoid any CANCELLATIONS by clicking on this link: [WEBSITE] or call the office at [PHONE NO.], opt 2. Thank you.

51 m 6’2” 220lbs. Had my first AFib in January after a night with too much booze. Typical symptoms, went to ER. Shocked heart once, and back to normal. Met with cardiologist to go over stuff. Ultrasound on my heart shows no damage. Both times I entered AFib were the morning after a few drinks AND the day after doctors changed blood pressure meds.
The situation today is I’m in Cancun, went to the ER to confirm. They wanted to keep me for 3 days to give me meds and monitor. They said not right for the shock thing.
My insurance will only pay after the fact, and the wanted a 150,000 peso card hold to treat. ($10,000).
I have no symptoms. The only reason I thought to check with my little portable machine was my 40 minutes on the treadmill were a bit more difficult.
Sure enough, I’m Afib. Blood pressure still good. Not low like before. No dizziness like before. Not a symptom without strenuous exercise. My cardiologist is not available til tomorrow to get advice. If my Kardia machine wasn’t picking up the flutter and readin a fast heart rate I would not know I’m in AFib. My blood pressure machine doesn’t detect it and shows normal heart rate.
Are they any supplements or foods that are good. Should I go back for a 3 day stint in the ER tonight? Anything over the counter? I have access to beta blockers and ccb’s at the pharmacy next door. Dosing myself seems a bit stupid though.
(Only slightly kidding) Would a 110v of electricity help?
Any advice would be appreciated?? I have stopped all alcohol, and caffeine of course.
Currently only on baby aspirin and Diltazem 240
Heavier blood thinners were stopped last week.

As the title says, my CVS app had my 7.5mg listed as “on hold” since the prescription arrived in early April. Today, I went and checked and now it says “action required.” Is this a good sign by this being a potential PA required or am I going to be disappointed with another ‘out of stock’ answer. It says to “call pharmacy for options” but they’re very understaffed and not responding to calls well. I’ll get through to them… eventually.
I don’t know if this matters - I also tried to restart at 2.5 recently and that prescription is now “on hold.” When I called, they said it’s on hold bc it’s unavailable (when it’s been in stock for weeks, but that’s a shortage rant for another day). Maybe the system only allows one medication dosage to be “on hold” at a time and this is why the 7.5 has “action required?” TIA

Hey guys, quick question…does anyone know if my doctor sends a 3 month script to the pharmacy and the pharmacy only has 2 boxes, how that will work? Will the pharmacy accept my savings card for the two boxes? Been looking for 12.5 for over a month and finally found a location an hour and a half away… so if I can get both of the boxes they have in stock that would be preferred (I called already and that’s what they have available) since I’m making a decent trip over there. I usually pay $550 a box and I’ve never filled a 3 month script. Tyia !!

Anyone have any experience getting insurance to cover the Entyvio pen for CD? Currently on IV Entyvio and want to switch to the pen. Cigna denied my claim and is saying that I need to fail 3 other medications before they’ll cover it. Anyone have success appealing a denial?
ETA: apparently it’s CVS/Caremark that’s denying my prior authorization request since it’s a pharmacy benefit claim.

So, I waited 8 months before my prescription was filled. I have been on .25 for 8 weeks (Wed. I should take the 9th shot). My doctor prescribed the .5 and it came from my mail order pharmacy. On Saturday I got a text from CVS that they had my back ordered last refill. So now I have 4 weeks of .25 and 4 weeks of .5. I really feel like it's beneficial to raise the dose at this point, but I don't want to waste 4 shots. I'm thinking of alternating for the next four weeks. .5 this week, .25 the rest. This seems reasonable since it builds up in your system anyway. Has anyone tried anything similar? I'd try two .25 together, but I have a feeling my insurance company is going to delay the .5 refill because I just got a 4 week supply on Saturday.

My mom 53(f) has been struggling with her health these past couple years and has nerve related impairments in her lower extremities. We currently have one of AetnaCVSHealth’s gold plans for insurance.
They require a referral to see specialists. Every. Single. Time. You would assume that after going all the way to your PCP to get a referral the first time, any follow ups recommended by the specialist should be okay. However, this company will deny follow up appointments even as little as a week or two later — reported as follow ups to the insurance company— if there is no referral. I will get charged a $10 copay, and the insurance will fail to alert the hospital that a referral is required for coverage, leaving me having to pay for the full appointment on top of my $10. Specialist visits can cost upwards of $700 an hour for neurologists. I can understand if there has been a lot of time between visits or the visit isn’t technically a follow up but its getting to the point where we cant even schedule to view her test results without obtaining a referral first from her PCP which is absurd. We will have prescriptions for things like physical therapy from a specialist and they will not be covered by insurance if we dont go to our PCP first to get a referral from her as well.
They also will deny coverage if your providers are out of network however, their entire catalogue of in network providers is incorrect on their site. Im talking 80-90% whether its listing disconnected phone numbers, listing doctors that no longer accept the insurance, listing doctors that no longer operate at the mentioned address, listing the incorrect name of the healthcare institution, and so forth. This can make it extremely difficult to even get the right referral in the first place because they usually want the exact doctoprovider listed on the referral. Any variances can result in them denying your claim and charging you full price after making your copay.
They also deny surgeries and procedures even when they fall into their guidelines on what is considered “medically necessary”. It was so bad that the bille coder we were working with at the hospital expressed that this was the only insurance company that consistently denied quality of life surgeries. She even expressed to me that they tried to deny someone who needed brain surgery and would suffer a terrible quality of life without surgery (essentially vegetable state) because it wasnt technically necessary for them to survive… like yes you’d survive i guess but to what end?
They have no regard for the quality of life of their insurance holders and are consistently looking for ways to deny claims. I was wondering if there was any way to sue them for using these malicious tactics in order to keep themselves from having to cover pricey medical bills even when they should be covered based on their own parameters.
To my knowledge, aetna and cvs merged due to them both struggling to stay afloat financially, but if this is hindering them from offering reasonable healthcare they should NOT be allowed to participate in the marketplace. I also wanted to emphasize that this is our second year with them and it wasn’t nearly as difficult to use them last year (even with the incessant referrals) as it is this year. They seem to deny every other claim this time around.
Thank you in advance to anyone who may take the time to read and/or respond to this.
Edit: grammar, readability, and clarification.

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Hello insurance,
I'm currently facing a confusing situation with my dental insurance and billing, and I could really use some guidance from anyone who might have experience or expertise in this area.
Background: After being assigned a new dentist by Blue Shield, I was given a contact number (408-266-6144) to set up my initial appointment. The dental office I called, and subsequently visited for two appointments, was under a different name than listed but at the same address and phone number. This new office, according to their website, does not accept Blue Shield, yet they proceeded with my appointments without notifying me of this.

• First Visit (May 3rd): I had a basic check-up, X-rays, and evaluation but was later billed for out-of-network charges totaling $753, with no coverage applied.
• Second Visit (May 9th): This included cleaning and fillings. Although it was billed as in-network, the copays were inconsistent with my plan details. For example, resin-based composite fillings, typically a $30 copay per tooth, cost me $55 per tooth.

Insurance Details: My plan, a Family Dental HMO from Blue Shield of California, mentions $30 copays for basic fillings and no deductible. It's supposed to cover in-network services fully, but it turns out the provider was out-of-network on my first visit without informing me, and then mysteriously in-network on the second.
Additional Charges: Beyond the copay discrepancies, I was unexpectedly charged $285 on my debit card the day after my second appointment, in addition to the $25 copay I had paid during the visit.
I have already reached out to my insurance company and the dental office trying to make sense of these issues. Can anyone here help clarify potential next steps or share if they've experienced something similar? Any advice on how to navigate this with my insurance or the dental office would be greatly appreciated.

So i very much want to buy a PS plus subscription for pc cloud gaming and I used to buy the PS plus cards at walmart CVS and other stores, but I cannot seem to find them anymore. I only find the PS cards that add funds to your account, so would I be able to purchase a PS funds card and pay for the subscription that way?
Also, what is the difference between cards?
What is the best way to purchase PS plus premium subscription?

I was happy with my life (outside from CVS) as a staff pharmacist at my home store, and was just offered PMEL position from my DL. Has anyone done PMEL position? Does that mean I have to become a PM one day?

I’d love for any detractors to correct me!!
Now, there’s a couple talking points people tend to use to support this nonsense and I’ll talk about some here. If you can think of any more, talk about them in the comments!!
Some people (idiots) say you won’t be able to get a diagnosis if:

• you’re low income.

You’re in luck my friend!! There is hope. Some universities allow psych students, under the supervision of a professional, to do assessments, not something super in depth like an autism assessment, but easier to screen disorders. My therapist actually had this done on him and it was an in depth assessment too. And he was able to get his answers. It’s way cheaper than going to a full on professional. And it’s good, just not AS good. You can call ahead of time and ask the psych/therapist office how much the appointment will cost out of pocket. A lot of places are willing to give you a discount if you just ask to do a copay based off income. The reason why the costs tend to be so high (in the US) because insurance effs up the cost of everything. I’ve done this before. It’s generally cheaper than going through insurance. At my old therapy place, it was $50 an appointment with insurance. Without insurance it was $5 an appointment. Just don’t tell them you have insurance until you get the rate. Go to a non profit or state ran facility. Not nearly as glamorous as your private places, but if you’re desperate enough to self diagnose, take what you can get. One of my close friends goes to a non profit place and he gets therapy for free since they also base off income.

• you’re a woman or a POC

As a former woman myself, I can attest some psych professionals are sexist. But remember, a diagnosis CAN be changed as you talk to the person more and they get a proper history on you. I got a BPD misdiagnosis because I’m a trans man and I have bipolar disorder. I was dismissed. So I went to another professional who listened. After a couple appointments he was baffled on how I even got that diagnosis because I had maybe two symptoms? And those overlapped with my bipolar symptoms. It sucks. Anywho, enough talk about myself. But like in any serious situation, it’s up to you to advocate for yourself. Not in an ‘I HAVE THIS I KNOW I DO’ way. But in an ‘I don’t believe this diagnosis is right and here’s why’ way. This way works. Don’t be a know it all, they’ll just dismiss you.

• you don’t fit the stereotypical depiction of the disorder

Atypical presentations of disorders can exist, yes. But make sure you’re going to the RIGHT professional. See a neuropsychologist for an ADHD diagnosis. Not your damn GP. The neuropsychologist can spot the disorder from a mile away.

• your rights will be taken away

This just isn’t true.. you won’t lose your freedoms. A diagnosis can only help you, you don’t have to tell someone like your employer unless you’re a government employee. You can get accommodations and extra time off if you disclose your diagnosis.
What you can do instead of self-dx:

• accommodate yourself. Don’t feel shame for this. As long as you’re a nuisance
  
• track your symptoms and present it to a professional
  
• talk to diagnosed people for advice on how they treat their symptoms if you’re also experiencing them.
  
• if your symptoms are so extreme, come up with a crisis plan. I keep a small bag of my meds with me everywhere I go, my insurance card/ card with my meds and doses and my emergency contact info in my wallet. If I can be prepared, you likely can too, especially if you’re an adult.