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Swe-Care Ovulation Test Kit

NAFDAC REG NO: A3-101332 Médicament

Enregistré auprès de NAFDAC. Enregistrement actifAs of 6 November 2026 · synced automatically from official sources.
Produit
Swe-Care Ovulation Test Kit
Numéro NAFDAC
A3-101332
Principe actif
Test Kit
Dosage
N/A
Forme
N/A
Conditionnement
5's
Fabricant
Non répertorié
Déposant / Titulaire :
Nolly V. Global Nig Ltd
Approuvé
29 Aug 2024
Statut
Actif Vue sur NAFDAC ↗
Enregistrement valable jusqu'au
27 Aug 2029
Alertes OMS
Non trouvé
Community reports
None
Times checked
0

About the medicine: Test kit: uses, dosage and brands worldwide

What we found

  • Swe-Care Ovulation Test Kit is on the NAFDAC register with an active registration (A3-101332). A valid number alone does not prove a pack is genuine — counterfeiters copy real numbers, so also check the expiry date, seal and print quality.

Generated automatically from the NAFDAC register, WHO alerts and community data as of today. This is not medical advice. Always follow your doctor or pharmacist.

How to use Swe-Care Ovulation Test Kit

Ce que dit la notice officielle. Si un médecin vous l'a prescrit, suivez l'ordonnance. La notice de votre boîte prime si elle est différente.

Mise en garde grave : RISK OF SEVERE BRONCHOSPASM Mannitol, the active ingredient in ARIDOL, acts as a bronchoconstrictor and may cause severe bronchospasm. Bronchial challenge testing with ARIDOL is for diagnostic purposes only. Bronchial challenge testing with ARIDOL should only be conducted by trained professionals under the supervision of a physician familiar with all aspects of the bronchial challenge test and the management of acute bronchospasm. …
Pour qui

ARIDOL is indicated for the assessment of bronchial hyperresponsiveness in adult and pediatric patients 6 years of age or older who do not have clinically apparent asthma. Limitations of Use: ARIDOL is not a standalone test or a screening test for asthma. Bronchial challenge testing with ARIDOL should be used only as part of a physician's overall assessment of asthma. ARIDOL is a sugar alcohol indicated for the assessment of bronchial hyperresponsiveness in adult and pediatric patients 6 years of age or older who do not have clinically apparent asthma. ( 1 ) Limitations of Use: ARIDOL is not a standalone test or a screening test for asthma. …

Comment le prendre et à quelle fréquence
  • For Oral Inhalation Use Only One ARIDOL test kit contains dry powder mannitol capsules in graduated doses and a single patient use inhaler necessary to perform one bronchial challenge test
  • The mannitol capsules supplied in the ARIDOL kit are to be used with the single patient use inhaler device
  • Discard the inhaler after use
  • Capsule contents are to be inhaled in increasing dosage until either a positive response (15% reduction in FEV 1 from baseline or a 10% incremental reduction in FEV 1 between consecutive doses) is achieved or all capsules are inhaled (maximum total dose 635mg) Starting and maximum dose is the same for children (≥6 years old) and adults Bronchial Challenge Test Kit Overview ARIDOL is a bronchial challenge test kit containing the required capsules of dry powder mannitol for oral inhalation in graduated doses with the supplied single patient use inhaler necessary to perform one bronchial challenge test
  • Do not swallow ARIDOL capsules
  • The airway response to bronchial challenge testing with ARIDOL is measured using forced expiratory volume in one second (FEV 1 )
  • Prior to bronchial challenge testing with ARIDOL, standard spirometry should be performed and the reproducibility of the resting FEV 1 established
  • Administration Instructions An overview of the testing procedure can be found below
  • The ARIDOL bronchial challenge test should only be used with the provided inhaler
  • All remaining unused (opened and unopened) blister packs and the inhaler should be properly discarded at the completion of the test. …
Strengths it comes in

Inhalation powder: 0 mg, 5 mg, 10 mg, 20 mg, and 40 mg of mannitol dry powder per capsule in a bronchial challenge test kit. Each kit contains one, single patient use, dry powder inhaler device and 3 consecutively numbered foil blister packs containing a total of 19 capsules of mannitol for oral inhalation as described below: Blister pack "1" : Marked 1 - 1 x empty clear capsule printed with two w …

Children
  • The safety and effectiveness of ARIDOL for the assessment of bronchial hyperresponsiveness in adult and pediatric patients 6 years of age or older who do not have clinically apparent asthma have been established
  • The use of ARIDOL for this indication is supported by evidence from two clinical studies that included 246
  • Pediatric patients 6 to 17 years of age [ see Clinical Studies ]. …
Older adults

Clinical studies of ARIDOL did not include sufficient numbers of patients 50 years of age and older to determine whether they respond differently from younger adult patients.

While you are taking it
  • Severe Bronchospasm Prior to administration patients should be informed of the potential for bronchial challenge testing with ARIDOL to cause severe bronchospasm and of the potential symptoms they may experience [see Warnings and Precautions ]
  • Patients with Certain Co-morbid Conditions Bronchial challenge testing with ARIDOL should be performed with caution in patients having severe cough, ventilatory impairment, spirometry-induced bronchoconstriction, hemoptysis of unknown origin, pneumothorax, recent abdominal or thoracic surgery, recent intraocular surgery, unstable angina, or active upper or lower respiratory tract infection or other conditions that may worsen with the use of a …
Talk to a doctor first if
  • ARIDOL is contraindicated in: Patients with known hypersensitivity to mannitol or to the gelatin used to make the capsules Patients with conditions that may be compromised by induced bronchospasm or repeated spirometry maneuvers
  • Some examples include: aortic or cerebral aneurysm, uncontrolled hypertension, recent myocardial infarction or cerebral vascular accident [ see Warnings and Precautions ]. …
Medicines it may not mix with

No formal drug-drug interaction studies were conducted with mannitol, the active ingredient in ARIDOL.

Warnings

& PRECAUTIONS Severe bronchospasm: ARIDOL may cause severe bronchospasm in susceptible patients. Administer by trained professionals under the supervision of a physician. Medications and equipment to treat severe bronchospasm must be present in the testing area. ( 5.1 ) Subjects with co-morbid conditions: Use with caution in patients with conditions that may increase sensitivity to the bronchoconstricting or other potential effects of ARIDOL such as: severe cough, ventilatory impairment, unstable angina, or active upper or lower respiratory tract infection that may worsen with use of a bronchial irritant. …

Effets secondaires possibles

The following clinically significant adverse reaction is described elsewhere in the labeling: • Severe Bronchospasm [ see Warnings and Precautions ( 5.1 )]. Most common adverse reactions (rate ≥1%) were headache, pharyngolaryngeal pain, throat irritation, nausea, cough, rhinorrhea, dyspnea, chest discomfort, wheezing, retching and dizziness. ( 6.1 ) To report SUSPECTED ADVERSE REACTIONS, contact Methapharm, Inc. …

Pregnancy and breastfeeding

8.1 Pregnancy Risk Summary There are no available human data regarding inhaled mannitol to evaluate a drug-associated risk for major birth defects, miscarriage, or other adverse maternal or fetal outcomes. Based on animal reproduction studies, no evidence of structural alterations was observed when mannitol was orally administered to pregnant rats and mice during organogenesis at doses up to approximately 20 and 10 times, respectively, the maximu …

If you take too much

Susceptible persons may experience excessive bronchospasm from an overdosage. If such bronchospasm occurs, immediately administer a short-acting inhaled beta-agonist and other medical treatments such as oxygen, as necessary.

En cas d'oubli

Prenez-le dès que vous y pensez, sauf s'il est presque l'heure de la dose suivante. Dans ce cas, sautez la dose oubliée. Ne prenez jamais deux doses à la fois pour compenser. Vérifiez votre notice, certains médicaments font exception.

From the official U.S. FDA label for this active ingredient. Your pack may have a different strength, so always read its leaflet. If a doctor prescribed it, follow the prescription. Ask a pharmacist if you are unsure. Label dated 2026-04-23.

Label for test kit, the active ingredient registered with NAFDAC.

NAFDAC recall & alert notices

Public Alert No. 033/2024 – Alert on the Recall of Radox Care + Moisturise Liquid Hand Wash due to presence of Butyphenyl Methylpropional (BMHCA) Content22 Aug 2024 · nafdac.gov.ngThe National Agency for Food and Drugs Administration and Control (NAFDAC) is notifying the public of the recall of Radox Care + Moisturise Liquid Hand Wash by the European Union (EU) in Brussels, Belgium.The product does not comply with the Cosmetic Products Regulation as it is said to contain Butyphenyl Methylpropion…Public Alert No.022/2021 – Update: FDA Recommends Transition from Use of Non-NIOSH-Approved and Decontaminated Disposable Respirators – Letter to Health Care Personnel and Facilities8 Jul 2021 · nafdac.gov.ng, The National Agency for Food and Drug Administration and Control (NAFDAC) has been informed that the U.S. Food and Drug Administration (FDA) is recommending health care personnel and facilities to transition away from crisis capacity conservation strategies, such as using non-NIOSH-approved disposable respirators, in…Important Covid-19 Vaccine Safety Communication To Healthcare Providers27 May 2021 · nafdac.gov.ng, Important Covid-19 Vaccine Safety Communication To Healthcare Providers KEY POINTS    Possible Rare Event, Severe Allergic Reactions (Anaphylaxis) and Thromboembolic Events with Some Covid-19 Vaccines (probably due to underlying medical conditions and use of certain medications). Possible contraindications with Non…Public Alert No: 39/2020 – Alert on Happy Ducts Compress, Cord Care and Goldenseal Powder by WishGarden Herbs Due to Bacterial Contamination30 Dec 2020 · nafdac.gov.ng, The National Agency for Food and Drug Administration and Control (NAFDAC) has received information from the US FDA about voluntary recall of some lots of Happy Ducts Compress, Cord Care and Goldenseal Powder by WishGarden Herbs. The recall is due to a possible supply chain contamination with the bacteria Cronobacter …

Compare the brands and batch numbers in these notices with your pack, or enter your batch number above.

Check your pack of Swe-Care Ovulation Test Kit

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Encore 3 vérifications gratuites aujourd'hui Official sources: U.S. FDA · EMA (EU) · Health Canada · WHO alerts

About Swe-Care Ovulation Test Kit

What is in Swe-Care Ovulation Test Kit?

Swe-Care Ovulation Test Kit contains Test Kit (NA), as na, according to its NAFDAC registration record.

Is Swe-Care Ovulation Test Kit registered with NAFDAC?

Yes. Swe-Care Ovulation Test Kit is listed on the NAFDAC register under registration number A3-101332, and its registration is active as of 6 November 2026.

Has Swe-Care Ovulation Test Kit been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Swe-Care Ovulation Test Kit in our automatically synced alert list.

How can I check that my pack of Swe-Care Ovulation Test Kit is genuine?

Run a free authenticity scan with the NAFDAC number A3-101332, 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.

How do I take Swe-Care Ovulation Test Kit?

Follow your prescription or the leaflet in your pack. The official label says: For Oral Inhalation Use Only One ARIDOL test kit contains dry powder mannitol capsules in graduated doses and a single patient use inhaler necessary to perform one bronchial challenge test. ( 2 ) The mannitol capsules supplied in the ARIDOL kit are to be used with the single patient use inhaler device ( 2 ). Discard the inhaler after use. Capsule contents are to be inhaled in i…

What is Swe-Care Ovulation Test Kit used for?

ARIDOL is indicated for the assessment of bronchial hyperresponsiveness in adult and pediatric patients 6 years of age or older who do not have clinically apparent asthma. Limitations of Use: ARIDOL is not a standalone test or a screening test for asthma. Bronchial challenge testing with ARIDOL should be used only as part of a physician's overall assessment of asthma. ARIDOL is a sugar alcohol ind (Summarised from the official U.S. FDA label for test kit. Always follow your doctor or pharmacist.)

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