CAUTION
Caution
is advised when consuming alcohol with Feluric. Please consult your doctor.
CONSULT YOUR DOCTOR
Feluric
may be unsafe to use during pregnancy. Although there are limited studies in
humans, animal studies have shown harmful effects on the developing baby. Your
doctor will weigh the benefits and any potential risks before prescribing it to
you. Please consult your doctor.
CONSULT YOUR DOCTOR
Feluric
is probably unsafe to use during breastfeeding. Limited human data suggests
that the drug may pass into the breastmilk and harm the baby.
UNSAFE
Feluric
may cause side effects which could affect your ability to drive. Feluric may
cause dizziness, sleepiness, blurred vision, numbness or tingling sensation.
This may affect your driving ability.
CAUTION
Feluric
should be used with caution in patients with severe kidney disease. Dose
adjustment of Feluric may be needed. Please consult your doctor. Limited
information is available regarding the use of Feluric in these patients.
CAUTION
Feluric
should be used with caution in patients with severe liver disease. Dose
adjustment of Feluric may be needed. Please consult your doctor. Limited
information is available regarding the use of Feluric in these patients.
Medicine
Overview of Feluric 40mg Tablet
Introduction
Feluric is a medicine used to treat and prevent gout. Gout happens when there is too much uric acid in your body and it forms into crystals which can appear around your joints leading to painful and swollen joints. This medicine helps to keep uric acid levels low. Feluric can be taken with or without food. You should keep taking it as recommended by your doctor even when you are not having a gout attack. If you stop, your symptoms may get worse because of the formation of more crystals in your joints. You can help yourself by making some changes to your diet (eg. avoiding alcohol and non-vegetarian foods) and drinking plenty of fluids. Some of the common side effects of this medicine are headache, diarrhea, nausea, skin rash and a temporary increase in gout symptoms (rapid onset of severe pain, warmth, and redness in the joint). However, do not stop taking it. Your doctor may advise you some painkillers and additional medicines to help you reduce or prevent these symptoms. Rarely, some people may get a severe allergic reaction (difficulty in breathing, hives, swelling of face and throat, weakness) which may need urgent medical attention. Also, tell your doctor right away if you get any symptoms of liver disease like persistent nausea, dark urine or yellowing of the eyes or skin. Before taking this medicine, let your doctor know if you have any heart problems, stroke, thyroid problems, or kidney or liver problems. If you are pregnant or breastfeeding, this medicine is best avoided. Check with your doctor. You will need regular blood tests while taking this medicine to check that your liver is working properly.
Uses of
Feluric
·
Gout
Side
effects of Feluric
Common
·
Diarrhea
·
Headache
·
Increased liver enzymes
·
Nausea
·
Skin rash
·
Gout flares
How to
use Feluric
Take
this medicine in the dose and duration as advised by your doctor. Swallow it as
a whole. Do not chew, crush or break it. Feluric may be taken with or without
food, but it is better to take it at a fixed time.
How
Feluric works
Feluric
is a xanthine oxidase inhibitor. It works by decreasing blood uric acid, which
is the chemical that causes gout.
What if
you forget to take Feluric?
If you
miss a dose of Feluric, take it as soon as possible. However, if it is almost
time for your next dose, skip the missed dose and go back to your regular
schedule. Do not double the dose.
Quick Tips
·
Your doctor has prescribed Feluric to reduce episodes of gout
attack.
·
Take it at the same time every day, with or without food.
·
Take plenty of fluids (2-3 litres) daily while on Feluric.
·
When you first start taking this medicine, you might have more
gout attacks. Do not stop Feluric on having an acute attack of gout as that
could make an attack worse.
·
Do not consume alcohol while taking this medicine as it may cause
your gout to flare up.
·
Stop taking this medicine and inform your doctor straight away
if you have symptoms like rash, itchiness, difficulties in breathing, fever or
swelling of limbs or face.
Brief
Description
Indication
Gout,
Hyperuricemia
Administration
May be
taken with or without food. May be taken w/o regard to antacid use.
Adult
Dose
Chronic Gout 40 mg/day PO initially; maintenance: 40-80 mg/day; increased if serum uric acid is >6 mg/mL after 2 weeks Hepatic impairment Mild to moderate (Child-Pugh class A or B): Dosage adjustment not necessary Severe (Child-Pugh class C): Data not available; use with caution
Child
Dose
Safety
and efficacy not established
Renal
Dose
Renal impairment Mild to moderate (CrCl 30-89 mL/min): Dosage adjustment not necessary Severe (CrCl <30 mL/min): Data not available; use with caution
Contraindication
Patients
being treated with azathioprine, mercaptopurine, or theophylline.
Mode of
Action
Febuxostat selectively inhibits xanthine oxidase, the enzyme that catalyses the conversion of hypoxanthine to xanthine to uric acid, thereby decreasing serum concentrations of uric acid.
Precaution
Cardiovascular death Patients with established cardiovascular
(CV) disease treated with febuxostat had a higher rate of CV death compared
with those treated with allopurinol in a CV outcomes study. Evaluate risks and
benefits when prescribing febuxostat or continuing treatment. Gout Flare: An
increase in gout flares is frequently observed during initiation of
anti-hyperuricemic agents, including Febustat. If a gout flare occurs during
treatment, Febustat need not be discontinued. Prophylactic therapy (i.e.,
non-steroidal anti-inflammatory drug (NSAID) or colchicine upon initiation of
treatment) may be beneficial for up to six months. Lactation: Unknown whether
drug is excreted into breast milk; use with caution
Side
Effect
>1%
Arthralgia,Elevated liver function test (LFT) results,Liver function
abnormalities,Nausea,Rash
Pregnancy
Category Note
Pregnancy Limited available data in pregnant women are
insufficient to inform a drug associated risk of adverse developmental outcomes
Animal data No adverse developmental effects observed in embryo-fetal
development studies with oral administration of febuxostat to pregnant rats and
rabbits during organogenesis at doses that produced maternal exposures up to 40
and 51 times, respectively, the exposure at the maximum recommended human dose
(MRHD) No adverse developmental effects observed in a pre- and postnatal
development study with administration of febuxostat to pregnant rats from
organogenesis through lactation at an exposure ~11 times the MRHD Lactation
There are no data on presence of febuxostat in human milk, effects on breastfed
infant, or on milk production; drug is present in rat milk Consider the
developmental and health benefits of breastfeeding along with mother’s clinical
need for therapy and any potential adverse effects on breastfed child from
therapy or from underlying maternal condition
Interaction
May increase plasma conc of mercaptopurine, azathioprine. Alteration of metabolism of xanthine oxidase substrate drugs (eg theophylline).
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