Vitabiotics Immunace Triggered Adverse Reactions in Diabetic and Non-Diabetic Users
I purchased Immunace tablets by Vitabiotics from a pharmacy located in Sosiani Building in Eldoret for my brother, who has diabetes. After taking the tablets for just one day about ten days ago, he experienced a sleepless night and a significant rise in his blood sugar levels, which caused serious concern, so we immediately stopped giving him the product. I then decided to use the remaining half of the tablets myself and started taking Immunace on February 26, 2026, in Nairobi. I took a total of five tablets over five days before stopping. During this time, I developed body discomfort, weakness, and episodes of sweating during cold nights, which were unusual for me. When I visited a physician, I was told that my blood pressure was at an alarming level and that my blood sugar levels were elevated. Based on this, I stopped taking Immunace immediately, as I became concerned about my health and the possibility of any permanent effects. I have not yet contacted Vitabiotics, the pharmacy, or any health authority, but I am planning to do so. Through this complaint, I request that Vitabiotics conduct a thorough investigation into this product and the specific batch supplied to the pharmacy in Sosiani Building in Eldoret, including a safety assessment of the reported reactions in both a diabetic patient and a non-diabetic user. I also request clear information on whether these effects could have any long-term or permanent consequences and what follow-up medical checks would be recommended in relation to the use of Immunace in this situation.





