Sertraline 100mg tablets

Nchi: Uingereza

Lugha: Kiingereza

Chanzo: MHRA (Medicines & Healthcare Products Regulatory Agency)

Nunua Sasa

Shusha Taarifa za kipeperushi (PIL)
20-01-2023
Shusha Tabia za bidhaa (SPC)
21-04-2023

Viambatanisho vya kazi:

Sertraline hydrochloride

Inapatikana kutoka:

DE Pharmaceuticals

ATC kanuni:

N06AB06

INN (Jina la Kimataifa):

Sertraline hydrochloride

Kipimo:

100mg

Dawa fomu:

Oral tablet

Njia ya uendeshaji:

Oral

Darasa:

No Controlled Drug Status

Dawa ya aina:

Valid as a prescribable product

Bidhaa muhtasari:

BNF: 04030300

Taarifa za kipeperushi

                                _ _
_ _
•
shortness of breath, nose bleed, breathing difficulty, possible
wheezing,
•
tarry stools, tooth disorder, inflammation of the oesophagus,
tongue problem, haemorrhoids, increased saliva, difficulty
swallowing, burping, tongue disorder,
•
eye swelling, hives, hair loss, itching, purple spots on skin, skin
problem with blisters, dry skin, face oedema, cold sweat,
•
osteoarthritis, muscle twitching, muscle cramps*, muscular
weakness,
•
increase in frequency of urination, problem urinating unable to
urinate, urinary incontinence, increase in urination, nighttime
urination,
•
sexual dysfunction, excessive vaginal bleeding, vaginal
haemorrhage, female sexual dysfunction,
•
swelling in legs, chills, difficulty walking, thirst,
•
increase in liver enzyme levels, weight decreased.
•
CASES OF SUICIDAL IDEATION AND SUICIDAL BEHAVIOURS HAVE
BEEN REPORTED DURING SERTRALINE THERAPY OR EARLY AFTER
TREATMENT DISCONTINUATION (SEE SECTION 2).
Rare (may affect up to 1 in 1,000 people):
•
diverticulitis, swollen lymph glands, decrease in clotting cells*,
decrease in white blood cells*,
•
severe allergic reaction,
•
endocrine problems*,
•
high cholesterol, problems controlling blood sugar levels
(diabetes), low blood sugar, increase in blood sugar levels*, low
blood salt*,
•
physical symptoms due to stress or emotions, terrifying
abnormal dreams*, drug dependence, sleep walking, premature
ejaculation
•
coma, abnormal movements, difficulty moving, increased
sensation, sudden severe headache (which may be a sign of a
serious condition known as Reversible Cerebral
Vasoconstriction Syndrome (RCVS))*, sensory disturbance,
•
spots in front of eyes, glaucoma, double vision, light hurts eye,
blood in the eye, unequal sized pupils*, vision abnormal*, tear
problem,
•
heart attack, light-headedness, fainting, or chest discomfort
which could be signs of changes in the electrical activity (seen
on electrocardiogram) or abnormal rhythm of the heart*, slow
heartbeat,
•
poor circulation of arms and legs,

                                
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Tabia za bidhaa

                                SUMMARY OF PRODUCT CHARACTERISTICS
1
NAME OF THE MEDICINAL PRODUCT
Sertraline 100mg Tablets
2
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each film-coated tablet contains 100 mg of sertraline (as
hydrochloride).
Excipient(s) with known effect:
Each film-coated tablet contains 87.42 mg lactose (as monohydrate) and
1.34
mg (0.058 mmol) sodium.
For the full list of excipients, see section 6.1.
3
PHARMACEUTICAL FORM
Film-coated tablet.
White to off-white, capsule shaped tablet scored on one side.
The tablet can be divided into equal doses.
4
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Sertraline is indicated for the treatment of:
Major depressive episodes. Prevention of recurrence of major
depressive episodes.
Panic disorder, with or without agoraphobia.
Obsessive compulsive disorder (OCD) in adults and paediatric patients
aged 6-17
years.
Social anxiety disorder.
Post traumatic stress disorder (PTSD)
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Posology
_Initial treatment _
_Depression and OCD _
Sertraline treatment should be started at a dose of 50 mg/day.
_Panic Disorder, PTSD, and Social Anxiety Disorder _
Therapy should be initiated at 25 mg/day. After one week, the dose
should be
increased to 50 mg once daily. This dose regimen has been shown to
reduce
the frequency of early treatment emergent adverse reactions
characteristic of
panic disorder.
_Titration _
_Depression, OCD, Panic Disorder, Social Anxiety Disorder and PTSD _
Patients not responding to a 50 mg dose may benefit from dose
increases.
Dose changes should be made in steps of 50 mg at intervals of at least
one
week, up to a maximum of 200 mg/day. Changes in dose should not be
made
more frequently than once per week given the 24-hour elimination half
life of
sertraline.
The onset of therapeutic effect may be seen within 7 days. However,
longer
periods are usually necessary to demonstrate therapeutic response,
especially
in OCD.
_Maintenance _
Dose during long-term therapy should be kept at the lowest effective
level,
with subsequent
adjustment depending
                                
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