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Nasalide Side Effects, and Drug Interactions - Flunisolide (Nasal Spray)
ADVERSE REACTTIONS
The adverse events rates
listed below are based on symptoms spontaneously reported in multidose
controlled clinical trials in comparing NASAREL and NASALIDE for treatment
of allergic rhinitis. In patients receiving NASAREL the most common
adverse events were transient aftertaste (17%) and transient nasal burning
and stinging (13%). These symptoms did not usually interfere with
treatment.
Adverse Event Rates for
NASAREL:
Incidence Greater than 1%
(probably causally related)
Respiratory: Nasal
burning/stinging (13%), epistaxis *, nasal dryness, pharyngitis, cough
increased
Gastrointestinal: Nausea
Special
Senses: Aftertaste (17%)
Incidence 1% or Less
(probably causally related)
Respiratory: Hoarseness
Special Senses: Abnormal sense of smell
Incidence 1% or Less (causal relationship unknown) *
Respiratory: Sinusitis
Adverse Event
Rates for NASALIDE:
Incidence Greater than 1%
(probably causally related)
Respiratory: Nasal
burning/stinging (44%), epistaxis *, nasal dryness *, pharyngitis *, cough
increased
Gastrointestinal: Nausea
Special
Senses: Aftertaste (8%)
Incidence 1% or Less
(probably causally related)
Respiratory: Hoarseness,
nasal ulcer
Incidence 1% or Less (causal relationship
unknown) †
Respiratory: Sinusitis
________________________________________
*Incidence of reported reaction between 3% and 9%. Those reactions
occurring in less than 3% of the patients are unmarked.
† Reactions
occurred under circumstances where the causal relationship has not been
clearly established; they are presented as alerting information for
physicians.
Cases of growth suppression have been reported for
intranasal corticosteroids (including NASAREL) (see PRECAUTIONS, Pediatric
Use section).
DRUG INTERACTIONS
No information provided.
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