Generated automatically from the NAFDAC register, WHO alerts and community data as of today. Not medical advice — always follow your doctor or pharmacist.
From the official U.S. FDA label for budesonide, the active ingredient registered with NAFDAC.
s Temporarily relieves these symptoms of hay fever or other upper respiratory allergies: • nasal congestion • runny nose • itchy nose • sneezing
Nasal allergy symptom reliever
you have, or come into contact with someone who has, chickenpox, measles or tuberculosis you have or develop symptoms of an infection such as persistent fever you have any change in vision you have severe or frequent nosebleeds
in children under 6 years of age if you have ever had an allergic reaction to any of the ingredients
Do not use in children under 6 years of age if you have ever had an allergic reaction to any of the ingredients Ask a doctor before use if you have had recent nose ulcers or nose surgery have had a nose injury that has not healed are using a steroid medicine for asthma, allergies or skin rash have an eye infection have or had glaucoma or cataracts When using this product the growth rate of some children may be slower some symptoms may get better on the first day of treatment. It may take up to two weeks of daily use to feel the most symptom relief. …
If pregnant or breast-feeding , ask a health professional before use.
Add the expiry date printed on your pack for a full Trust Score — or look up uses, side effects and cheaper generics.
Symbicort 160/4.5 mcg Turbuhaler contains Budesonide; Formoterol Fumarate Dihydrate (160 mcg/Inhalation; 4.5 mcg/Inhalation), as inhalation powder, according to its NAFDAC registration record.
Yes. Symbicort 160/4.5 mcg Turbuhaler is listed on the NAFDAC register under registration number A4-7007, and its registration is active as of 5 November 2026.
No WHO falsified or substandard medical product alert currently matches Symbicort 160/4.5 mcg Turbuhaler in our automatically synced alert list.
Run a free authenticity scan with the NAFDAC number A4-7007, your pack's expiry date and batch number to get a Trust Score, compare the pack with the NAFDAC record (ingredient, strength, form, manufacturer), and buy only from licensed pharmacies.
s Temporarily relieves these symptoms of hay fever or other upper respiratory allergies: • nasal congestion • runny nose • itchy nose • sneezing (Summarised from the official U.S. FDA label for budesonide. Always follow your doctor or pharmacist.)
Reviews are personal experiences from RxVerify users, not medical advice. Report side effects to your doctor and to NAFDAC.