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Home / Registered in Nigeria / ABO & RhD Blood Grouping Kit (Solid Phase Method)

ABO & RhD Blood Grouping Kit (Solid Phase Method)

NAFDAC Reg. No. 03-3550 · Drug

Registered with NAFDAC. Registration activeAs of 31 October 2026 · synced automatically from official sources.
Product
ABO & RhD Blood Grouping Kit (Solid Phase Method)
NAFDAC number
03-3550
Active ingredient
Test Kit
Strength
NA
Form
NA
Pack size
20's
Manufacturer
Not listed
Applicant (holder)
Insight Health Consulting Limited
Approved
11 May 2021
Status
Inactive View on NAFDAC ↗
Registration valid to
6 May 2026
WHO alerts
None found
Community reports
None
Times checked
0

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

What we found

  • ABO & RhD Blood Grouping Kit (Solid Phase Method) is on the NAFDAC register with an active registration (03-3550). 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 ABO & RhD Blood Grouping Kit (Solid Phase Method)

What the official label says. If a doctor prescribed it, follow the prescription. Your pack's leaflet comes first if it is different.

Serious warning: 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. …
Who it is 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 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. …

How to take it and how often
  • 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. …

Possible side effects

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.

If you miss a dose

Take it when you remember, unless it is nearly time for the next dose. Then skip the missed one. Never take two doses at once to make up for it. Check your leaflet, as some medicines are different.

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.

Check your pack of ABO & RhD Blood Grouping Kit (Solid Phase Method)

Add the expiry date on your pack for a full Trust Score.

Or take photos of the pack
3 free checks left today Official sources: U.S. FDA · EMA (EU) · NAFDAC · WHO alerts

About ABO & RhD Blood Grouping Kit (Solid Phase Method)

What is in ABO & RhD Blood Grouping Kit (Solid Phase Method)?

ABO & RhD Blood Grouping Kit (Solid Phase Method) contains Test Kit (NA), as na, according to its NAFDAC registration record.

Is ABO & RhD Blood Grouping Kit (Solid Phase Method) registered with NAFDAC?

Yes. ABO & RhD Blood Grouping Kit (Solid Phase Method) is listed on the NAFDAC register under registration number 03-3550, and its registration is active as of 31 October 2026.

Has ABO & RhD Blood Grouping Kit (Solid Phase Method) been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches ABO & RhD Blood Grouping Kit (Solid Phase Method) in our automatically synced alert list.

How can I check that my pack of ABO & RhD Blood Grouping Kit (Solid Phase Method) is genuine?

Run a free authenticity scan with the NAFDAC number 03-3550, 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 ABO & RhD Blood Grouping Kit (Solid Phase Method)?

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 ABO & RhD Blood Grouping Kit (Solid Phase Method) 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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