Tabulated list of adverse reactions
Undesirable effects are listed by MedDRA System Organ Classes.
Assessment of undesirable effects is based on the following frequency groupings:
Very common: ≥ 1/10
Common: ≥ 1/100 to <1/10
Uncommon: ≥ 1/1,000 to <1/100
Rare: ≥ 1/10,000 to <1/1,000
Very rare: <1/10,000
Not known: cannot be estimated from the available data
System Organ Class | Frequency | Undesirable Effect |
Immune system disorders | Not known | • anaphylaxis |
Nervous system disorders | Not known | • temporary hyposmia • temporary ageusia |
Ear and labyrinth disorders | Not known | • ototoxicity1 |
Skin and subcutaneous tissue disorders | Not known | • Irritative skin reactions • skin sensitisation |
Renal and urinary disorders | Not known | • nephrotoxicity |
General disorders and administration site conditions | Not known | • application site discolouration |
1Use with caution in children, elderly patients and patients with impaired hearing (see Section 4.4 'Special warnings and precautions for use').
Reporting of suspected adverse reactions
Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via the Yellow Card Scheme at: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.