Soņodor Ū 50 mg, Diphenhydramine HCI
Each tablet contains:
Active ingredients: Diphenhydramine (DCI)
HCI, 50 mg.
Excipients: Lactose, microcrystalline cellulose,
stearic acid, colloidal anhydrous silica and
magnesium stearate, c.s.
PHARMACEUTICAL FORM AND PACKAGING Dividable Sleeping pills for oral use. SOŅODOR Sleeping pills is available
in packs of 10 or 16 tablets
ACTIVITY
The active ingredient, Diphenhydramine HCI,
is an effective antihistamine which has a
sleep inducing effect that reduces the time
to fall a sleep and gives more depth to your
sleep.
INDICATIONS
SOŅODOR is used to symptomatically alleviate
occasional insomnia, in particular when it
is difficult to get to sleep, if you feel
restless, are woken several times while you
sleep or woken early in the morning.
CONTRAINDICATIONS
SOŅODOR is not recommended in cases of asthma,
glaucoma (increase in intraocular pressure),
urinary difficulties due to prostate problems
or people with any type of hypersensitivity
background. It should not be taken if pregnant
or breastfeeding.
Fluoxetine must not be combined with monoamine
oxidase inhibitors (MAOI). Treatment of fluoxetine
should only be started 14 days after discontinuation
of a MAOI. At least 5 weeks should elapse
after discontinuing fluoxetine treatment before
starting a MAOI.
PRECAUTIONS
SOŅODOR Sleeping pills should only be taken before going
to sleep. It should not be taken for a longer
period of time than one week. Children under
18 should not use SOŅODOR, unless recommended
by a doctor because insomnia can be a symptom
of a more serious illness. Reduce the dosage
if somnolence is experienced the morning after.
INTERACTIONS
SOŅODOR Sleeping pills should not be taken in conjunction
with alcohol, sedatives, tranquilizers or
other nervous system depressor drugs, for
this can increase the effect. MAOI (Monoamine
oxidase inhibitor) antidepressants may extend
and intensify the anticholinergic effects
of the diphenhydramine therefore if you are
taking any of these medications please consult
your doctor before using SOŅODOR. If you are
taking any other medication you should consult
your doctor before taking this product.
WARNING
Pregnancy & lactation: Do no take SOŅODOR Sleeping tablets during pregnancy, specially during
the first or last quarter, unless the doctor
believes that the benefits justify the possible
risks. You must contact your doctor before
using SOŅODOR during the period of lactation.
Important for women: If you are pregnant
or think you could be, consult your doctor
before taken this medication. Taking medication
during pregnancy may be dangerous for the
embryo or foetus and must be supervised by
your doctor.
Effects on ability to drive: This preparation
causes drowsiness and you should therefore
avoid driving any vehicle or operating dangerous
machinery if taking SOŅODOR.
Use in children: Children under 12
years should NOT take SOŅODOR.
Diagnostic interferences: SOŅODOR may affect
skin examinations which use allergen. It is
recommended you cease using this medication
at least 3 days before starting these examinations
and inform your doctor.
DOSAGE
Oral. Swallow the tablet with some form of
liquid. Adults: The recommended dosage is
1 tablet per day, 20-30 minutes before going
to bed. Adolescents from 12-18 years old:
The recommended dosage is ― tablet (25 mg).
OVERDOSE AND ITS TREATMENT
In case of overdose or a massive partake of
tablets call the nearest hospital or local
poison control center.
SIDE EFFECTS
Ocasionally you could experience dry mouth,
loss of appetite, constipation or blurred
vision. In most cases the side effects mentioned
are mild and stopping the treatment has not
been necessary. Although, if you observe these
or any other side effects which are attributed
to taking this medication, consult your doctor
or pharmacist.
STORAGE
Store at room temperature.
EXPIRY
Do not use this medication after expiry date
indicated on the package.
ALL MEDICATIONS MUST BE KEPT OUT OF THE REACH
OF CHILDREN
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