Concerns About My Reandron Injection Experience
As a trans man, I receive an injection of Reandron 1000 into my glute every 12 weeks. I've undergone this procedure several times, always performed by skilled nurses. However, on my latest visit, my doctor opted to administer the injection personally. It was apparent from the outset that he was somewhat inexperienced. While preparing the medication, he ended up with a significant amount of air in the syringe while attempting to extract every last drop. Although he successfully removed the air, it seemed that the volume of solution in the syringe exceeded the normal amount. Additionally, he was not aware that I should lie down for the procedure; he intended for me to remain standing, but I chose to lie down myself for comfort. The injection was administered far too rapidly, causing considerable pain—much worse than I had ever experienced before. After the injection, there was slight bleeding, which had never occurred in my previous injections. The area feels peculiar; the pain is sharp and intermittent, accompanied by an unusual warmth. Initially, I considered asking for a nurse to do the injection instead, but I reasoned that a doctor should be competent in this aspect. Clearly, that wasn't the case. I'm now left wondering what the implications of this might be. Should I be concerned about this experience? What should I anticipate moving forward?
Answers (1)
3/29/2025, 1:10:42 AM
OpenHealth AI
I'm sorry to hear about your challenging experience with the Reandron injection. It's understandable that you're feeling concerned after what you described, especially since this was a departure from your usual care. Let’s break down your situation and discuss what you can do next.
Key Points:
- Injection Technique: Rapid administration and excess air or volume can lead to discomfort and other complications.
- Current Symptoms: Sharp pain, warmth, and slight bleeding are important to monitor.
- Next Steps: It's essential to keep an eye on your symptoms and manage discomfort.
Explanation:
-
Injection Technique: The way injections are given can affect your comfort and the medication’s effectiveness. Rapid injection can cause tissue trauma, leading to pain and localized inflammation. Over-extraction leading to excessive air can potentially introduce air bubbles, although these usually don’t lead to any major issues if handled properly.
-
Symptoms: The sharp pain and warmth you're experiencing could be signs of irritation or minor local inflammation. Slight bleeding can occur if the needle hasn't been handled properly, but it should resolve without concern as long as it's minimal.
Next Steps:
-
Monitor Symptoms: Keep a close eye on the injection site over the next few days. Look for any significant changes such as increasing redness, warmth, swelling, or development of a fever, as these could warrant urgent attention.
-
Pain Management: You can use over-the-counter pain relief like ibuprofen or acetaminophen to manage discomfort, as directed on the packaging. Applying a cold compress to the area can also help reduce swelling and alleviate pain.
-
Follow Up: If symptoms worsen or do not improve within a week, consider reaching out to a healthcare professional for further evaluation. Describe your experience and symptoms clearly; this can help them understand your situation.
-
Future Injections: For your future injections, don't hesitate to express your concerns. If you feel more comfortable with a nurse performing the injection, communicate that preference to your healthcare provider. You deserve to feel safe and supported during your treatment.
Conclusion:
It's normal to feel uneasy after an experience like this, but by monitoring your symptoms and managing discomfort, you can take proactive steps. Prioritize your communication in the future to ensure that your care aligns with your comfort and expertise needs. You're doing the right thing by seeking clarity and support—your health and well-being are important. If you have any further questions or updates about your recovery, feel free to ask.
Related Questions
Examining the Safe Use of Narcan in Healthy Individuals
As someone with red hair, I’ve come across studies suggesting that individuals with this hair color may have a higher tolerance for pain. I recently stumbled upon research discussing how an eccentric scientist administered naltrexone to some red mice, resulting in a reduction of their pain threshold to what is considered typical. This seemed to correlate with a gene that influences the body's opioid receptors. I'm curious about trying Narcan to determine if it has any noticeable effects—I'm not concerned about the placebo effect—but I'm uncertain if it would have adverse effects on me since I don’t have any opioid dependency. To give you an overview of my health profile: I’m a 27-year-old male, weigh 160 pounds, stand 6 feet tall, and I’m currently not on any medication nor do I have any history of medical issues. I appreciate any insights!
Hydroxychloroquine Prescription Following Low C4 Levels: Should I Continue?
Demographic Information: 19 years old, Assigned Female at Birth. Medical History: Diagnosed with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), postural orthostatic tachycardia syndrome (POTS), reactive gastropathy of unknown origin, obsessive-compulsive disorder (OCD), autism spectrum disorder (ASD), and major depressive disorder (MDD). Some of my healthcare professionals suspect mast cell activation syndrome (MCAS), though I have not been formally diagnosed. Current Medications: I am currently taking 250 mg of clomipramine, 15 mg of memantine, 1 mg of clonazepam, 30 mg of loratadine, 40 mg of famotidine, 30 mg of propranolol, 15 mg of midodrine, 6 mg of naltrexone, and 200 mg of hydroxychloroquine. Additionally, I use iron and vitamin C supplements to address low ferritin levels and take 3 mg of melatonin as needed for sleep. Several months back, I consulted a rheumatologist upon recommendation due to unexplained rashes, joint swelling, and discomfort that couldn't be attributed to my current conditions (I initially believed they were linked to ME/CFS, but my ME specialist had doubts). Despite blood work showing no indicators of autoimmune disorders—such as normal levels for ESR, CRP, ANA, and RF—I was still referred to rheumatology. The rheumatologist conducted further extensive blood testing and subsequently prescribed hydroxychloroquine. He suggested I may have undifferentiated connective tissue disease (UCTD) but did not formally diagnose me. While I value his expertise, I want to ensure that I am only taking necessary medications. My apprehension stems from the fact that, among 18 blood tests performed, complement C4 was the only abnormality, which was recorded as slightly low. The battery of tests included assessments such as creatine kinase, a myomarker panel, HLA association panel (including celiac screening), comprehensive metabolic panel (CMP), complete blood count (CBC), ESR, CRP, anti-CCP, ANA, anti-dsDNA antibodies, anti-RNP antibodies, anti-Scl70 antibodies, anti-centromere antibodies, anti-Sm antibodies, anti-Ro antibodies, anti-La antibodies, and complement C3, alongside C4. I have been on hydroxychloroquine for three months and have noticed some improvements: although my fatigue persists, the rashes on my hands and wrists appear less severe, my fingers look slimmer, and joint pain has diminished. This does lend some reassurance about continuing the medication; however, I am concerned that these benefits could be attributed to either a placebo effect or the low-dose naltrexone rather than the hydroxychloroquine itself. My primary worry is the potential adverse effects of using hydroxychloroquine if it is not warranted for my condition. Are there specific signs I should monitor or indications suggesting that this medication might not be necessary? Should I alleviate my concerns, or is there reason to be cautious? Any insights would be immensely helpful, thank you!
Seeking Guidance on Hormonal Treatment as a Trans Man
I am a 21-year-old transgender man (FTM). About a year ago, I began receiving testosterone injections using a product called Testoviron, administered at a dosage of 125mg biweekly. During my most recent appointment with my endocrinologist, we chose to switch to an alternative injection called Nebido, which is a 250mg dose given every 12 weeks. My concern is whether extending the interval between these injections will slow my overall progress. Additionally, I've heard it may be necessary to have a second shot six weeks after the initial one to enhance the effectiveness of the treatment. After reading some online, I noticed that this advice is common; however, I feel uncertain as my endocrinologist appears to have limited experience working with transgender patients. This has left me anxious about the potential effects of the hormonal therapy. I would greatly appreciate any insights or advice on this matter.
Chest Discomfort with Red Marks
Over the past year, I have developed red patches predominantly on my upper chest and occasionally on my neck. My physician suspects that this could be linked to anxiety. These marks often become painful upon contact and sometimes provoke an itch. Although I’m uncertain if it’s connected, I also experience occasional discomfort in my chest, particularly around the sternum and collarbone areas. I’m concerned that there might be a misdiagnosis and that an underlying issue could be present. Has anyone else faced a similar situation or discovered the underlying cause of their symptoms? I’m a 24-year-old male who does not smoke, consume alcohol, or use drugs.
Is it Safe to Reintroduce Birth Control After a Smoking Break?
A 45-year-old woman has recently quit smoking after a 7-month period during which she also took Effexor. Due to the combination of medication and smoking, she decided to halt her hormonal birth control along with Effexor. Now, with a month of being smoke-free and currently taking Wellbutrin and Vyvanse, she feels confident about her progress and is contemplating resuming her birth control pills, specifically Seasonale. Her medical history reveals no complications such as blood clots, and her doctor initially approved her to restart the medication. However, after further consideration, the physician sought the opinion of an ObGyn for confirmation. The woman is eagerly awaiting feedback from the specialist, ideally before she intends to begin her birth control again this coming Sunday, which coincides with the start of her menstrual cycle. Since Seasonale is designed for extended use, this will already lead to postponing her period by three months, and any delay in resuming the pill could extend that timeline further by another 3.5 months. She notes that the mini-pill may not effectively assist with managing her PMS cravings, making it an unfavorable choice. The woman is reaching out for guidance on the appropriate course of action. Any insights would be greatly appreciated!