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(Rx)
Brand and Other Names:Lyrica, Lyrica CR
Classes: Analgesics, Other;
Anticonvulsants, Other;
Fibromyalgia Agents
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Sections
Sections pregabalin
Dosing & Uses
Interactions
Adverse Effects
Warnings
Pregnancy
Pharmacology
Administration
Images
Patient Handout
Formulary
capsule: Schedule V
25mg
50mg
75mg
100mg
150mg
200mg
225mg
300mg
20mg/mL
82.5 mg
165 mg
330 mg
Regular-release capsules
Initial: 50 mg PO q8hr
Maintenance: May increase to 100 mg PO q8hr within 1 week, as needed; not to exceed
300 mg/day
Extended-release tablets
Postherpetic Neuralgia
Regular-release capsules
Extended-release tablets
Maintenance: May increase to 150mg q12hr after 1 week as needed; recommended dose is 300-
400 mg/day
Owing to dose-dependent adverse reactions, doses >450 mg/day are not recommended
Maintenance: Based on clinical response and tolerability, may increase dose in weekly
increments, not to exceed 600 mg/day
Efficacy of adjunctive pregabalin in patients taking gabapentin has not been evaluated in
controlled trials; consequently, no dosing recommendations can be made when pregabalin is
used with gabapentin
Initial: 75 mg PO q12hr (150 mg/day); may increase within 1 week to 300 mg/day PO divided
q12hr
If there is insufficient pain relief after 2-3 weeks and 300 mg/day dose is tolerated, may increase
dose again up to 600 mg/day PO divided q12hr
Dosage Modifications
Dosing Considerations
capsule: Schedule V
25mg
50mg
75mg
100mg
150mg
200mg
225mg
300mg
20mg/mL
Indicated as adjunctive therapy for treatment of partial onset seizures in patients aged ≥1 month
11 kg to <30 kg
o Initial: 3.5 mg/kg/day PO divided q8hr (for 1 month to 4 years) or q8-12hr (for ≥4
years)
o Maintenance: Based on clinical response and tolerability, may increase dose in
weekly increments, not to exceed 14 mg/kg/day
≥30 kg
o Initial: 2.5 mg/kg/day PO divided q8-12hr
o Maintenance: Based on clinical response and tolerability, may increase dose in
weekly increments up to 10 mg/kg/day (not to exceed 600 mg/day)
≥17 years
Fibromyalgia
The primary efficacy endpoint of change from baseline to Week 15 in mean pain intensity
(derived from an 11-point numeric rating scale) showed numerically greater improvement for the
pregabalin-treated patients compared to placebo-treated patients, but did not reach statistical
significance
Dosage Modifications
Renal impairment: Use in children with compromised renal function has not been studied
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Interactions
Interaction Checker
No Results
No Interactions Found
Interactions Found
Contraindicated
Minor
Contraindicated (0)
benazepril
benazepril, pregabalin. Either increases toxicity of the other by Other (see comment).
Avoid or Use Alternate Drug. Comment: Coadministration results in additive risk of
developing angioedema of face, mouth, and neck. Angioedema may result in respiratory
compromise.
captopril
captopril, pregabalin. Either increases toxicity of the other by Other (see comment).
Avoid or Use Alternate Drug. Comment: Coadministration results in additive risk of
developing angioedema of face, mouth, and neck. Angioedema may result in respiratory
compromise.
enalapril
enalapril, pregabalin. Either increases toxicity of the other by Other (see comment).
Avoid or Use Alternate Drug. Comment: Coadministration results in additive risk of
developing angioedema of face, mouth, and neck. Angioedema may result in respiratory
compromise.
everolimus
everolimus, pregabalin. Either increases toxicity of the other by Other (see comment).
Avoid or Use Alternate Drug. Comment: Coadministration results in additive risk of
developing angioedema of face, mouth, and neck. Angioedema may result in respiratory
compromise.
fosinopril
fosinopril, pregabalin. Either increases toxicity of the other by Other (see comment).
Avoid or Use Alternate Drug. Comment: Coadministration results in additive risk of
developing angioedema of face, mouth, and neck. Angioedema may result in respiratory
compromise.
imidapril
lisinopril
lisinopril, pregabalin. Either increases toxicity of the other by Other (see comment).
Avoid or Use Alternate Drug. Comment: Coadministration results in additive risk of
developing angioedema of face, mouth, and neck. Angioedema may result in respiratory
compromise.
metoclopramide intranasal
pregabalin, metoclopramide intranasal. Either increases effects of the other by Other (see
comment). Avoid or Use Alternate Drug. Comment: Avoid use of metoclopramide
intranasal or interacting drug, depending on importance of drug to patient.
moexipril
moexipril, pregabalin. Either increases toxicity of the other by Other (see comment).
Avoid or Use Alternate Drug. Comment: Coadministration results in additive risk of
developing angioedema of face, mouth, and neck. Angioedema may result in respiratory
compromise.
perindopril
perindopril, pregabalin. Either increases toxicity of the other by Other (see comment).
Avoid or Use Alternate Drug. Comment: Coadministration results in additive risk of
developing angioedema of face, mouth, and neck. Angioedema may result in respiratory
compromise.
quinapril
quinapril, pregabalin. Either increases toxicity of the other by Other (see comment).
Avoid or Use Alternate Drug. Comment: Coadministration results in additive risk of
developing angioedema of face, mouth, and neck. Angioedema may result in respiratory
compromise.
ramipril
ramipril, pregabalin. Either increases toxicity of the other by Other (see comment). Avoid
or Use Alternate Drug. Comment: Coadministration results in additive risk of developing
angioedema of face, mouth, and neck. Angioedema may result in respiratory
compromise.
sirolimus
sirolimus, pregabalin. Either increases toxicity of the other by Other (see comment).
Avoid or Use Alternate Drug. Comment: Coadministration results in additive risk of
developing angioedema of face, mouth, and neck. Angioedema may result in respiratory
compromise.
temsirolimus
temsirolimus, pregabalin. Either increases toxicity of the other by Other (see comment).
Avoid or Use Alternate Drug. Comment: Coadministration results in additive risk of
developing angioedema of face, mouth, and neck. Angioedema may result in respiratory
compromise.
trandolapril
trandolapril, pregabalin. Either increases toxicity of the other by Other (see comment).
Avoid or Use Alternate Drug. Comment: Coadministration results in additive risk of
developing angioedema of face, mouth, and neck. Angioedema may result in respiratory
compromise.
Monitor Closely (122)
alprazolam
amitriptyline
amobarbital
amoxapine
benzhydrocodone/acetaminophen
brexanolone
brexanolone, pregabalin. Either increases toxicity of the other by sedation. Use
Caution/Monitor.
brexpiprazole
brompheniramine
buprenorphine
buprenorphine buccal
buprenorphine transdermal
pregabalin, buprenorphine transdermal. Either increases effects of the other by
pharmacodynamic synergism. Modify Therapy/Monitor Closely. Coadministration of
CNS depressants can result in serious, life-threatening, and fatal respiratory depression.
Use lowest dose possible and monitor for respiratory depression and sedation.
bupropion
buspirone
butabarbital
butalbital
butorphanol
cenobamate
cetirizine
chloral hydrate
chlordiazepoxide
chlorpheniramine
citalopram
clobazam
pregabalin, clobazam. Either increases effects of the other by Other (see comment).
Modify Therapy/Monitor Closely. Comment: Coadministration of CNS depressants can
result in serious, life-threatening, and fatal respiratory depression. Use lowest dose
possible and monitor for respiratory depression and sedation.
clomipramine
clonazepam
clorazepate
codeine
desipramine
desloratadine
desvenlafaxine
deutetrabenazine
dexchlorpheniramine
diazepam
dimenhydrinate
diphenhydramine
doxepin
doxylamine
duloxetine
escitalopram
esketamine intranasal
estazolam
eszopiclone
ethanol
fentanyl
fentanyl intranasal
fentanyl transdermal
fentanyl transmucosal
fexofenadine
fluoxetine
flurazepam
fluvoxamine
gepirone
pregabalin, gepirone. Either increases effects of the other by pharmacodynamic
synergism. Modify Therapy/Monitor Closely. Coadministration of CNS depressants can
result in serious, life-threatening, and fatal respiratory depression. Use lowest dose
possible and monitor for respiratory depression and sedation.
hydrocodone
hydromorphone
hydroxyzine
imipramine
isocarboxazid
lasmiditan
levocetirizine
levomilnacipran
levorphanol
loratadine
lorazepam
lumateperone
lurasidone
lurasidone, pregabalin. Either increases toxicity of the other by Other (see comment). Use
Caution/Monitor. Comment: Potential for increased CNS depressant effects when used
concurrently; monitor for increased adverse effects and toxicity.
maprotiline
meperidine
meprobamate
methadone
midazolam
midazolam intranasal
milnacipran
mirtazapine
morphine
nalbuphine
pregabalin, nalbuphine. Either increases effects of the other by pharmacodynamic
synergism. Modify Therapy/Monitor Closely. Coadministration of CNS depressants can
result in serious, life-threatening, and fatal respiratory depression. Use lowest dose
possible and monitor for respiratory depression and sedation.
nefazodone
nortriptyline
oliceridine
orlistat
oxazepam
oxycodone
oxymorphone
pregabalin, oxymorphone. Either increases effects of the other by pharmacodynamic
synergism. Modify Therapy/Monitor Closely. Coadministration of CNS depressants can
result in serious, life-threatening, and fatal respiratory depression. Use lowest dose
possible and monitor for respiratory depression and sedation.
paroxetine
pentazocine
pentobarbital
phenelzine
promethazine
protriptyline
ramelteon
remifentanil
remimazolam
samidorphan
secobarbital
sertraline
stiripentol
sufentanil
sufentanil SL
suvorexant
tapentadol
tasimelteon
temazepam
pregabalin, temazepam. Either increases effects of the other by pharmacodynamic
synergism. Modify Therapy/Monitor Closely. Coadministration of CNS depressants can
result in serious, life-threatening, and fatal respiratory depression. Use lowest dose
possible and monitor for respiratory depression and sedation.
tramadol
tranylcypromine
trazodone
triazolam
trimipramine
triprolidine
vilazodone
vortioxetine
zaleplon
zolpidem
Minor (0)
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Adverse Effects
Dose-dependent; percentages according to highest reported
>10%
Lyrica CR
Dizziness (3.4-17.1%)
Somnolence (0.5-11.4%)
Lyrica
Dizziness (8-45%)
Somnolence (lethargy, sluggishness, hypersomnia; 4-36%)
Peripheral edema (16%)
Ataxia (1-20%)
Fatigue (5-11%)
Xerostomia (1-15%)
Weight gain (16%)
Tremor (11%)
Blurred vision (1-12%)
Diplopia (12%)
1-10%
Lyrica CR
Vertigo (1-3.9%)
Headache (1.9-3.9%)
Vision blurred (0.5-3.7%)
Balance disorder (0.5-2.6%)
Weight increased (2.5-3.8%)
Fatigue (2.4-3.9%)
Constipation (2.7%)
Dry mouth (0.5-3.7%)
Nausea (3-3.4%)
Peripheral edema (3.8-4.9%)
Fatigue (1.4 -3.9%)
Joint swelling (1.9%)
Nasopharyngitis (1.4-1.5%)
ALT/AST increased (0.2-1.4%)
Diarrhea (1-1.4%)
Lyrica
Asthenia (5%)
Edema (8%)
Facial edema (<3%)
Hypotension (2%)
Neuropathy (2-9%)
Pain (5%)
Disorientation (<2%)
Constipation (5%)
Weight gain (4%)
Accidental injury (4%)
Abnormal thinking (2%)
Confusion (<7%)
Amnesia (<6%)
Vertigo (1-4%)
<1%
Addiction
Anemia
Diarrhea
Epididymitis
Esophagitis
Dysmenorrhea
Dystonia
Heart failure
Hirsutism
Uveitis
Postmarketing Reports
Angioedema
Creatinine kinase
Pneumonia
Viral infection
Bullous pemphigoid
Respiratory depression
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Warnings
Contraindications
Hypersensitivity
Cautions
Peripheral edema may occur; higher frequencies of weight gain and peripheral edema were
observed in patients taking both pregabalin and a thiazolidinedione antidiabetic agent compared
to patients taking either drug alone; monitor these patients for possible exacerbation of
congestive heart failure symptoms when using pregabalin
Pregabalin may cause dizziness and somnolence; inform patients that pregabalin may impair
their ability to perform tasks such as driving or operating machinery; concomitant use of
pregabalin with other central nervous system (CNS) depressants may exacerbate these effects;
for patients 1 month to less than 4 years of age, somnolence includes related terms lethargy,
sluggishness, and hypersomnia
Weight gain may occur; long-term cardiovascular effects of pregabalin-associated weight gain
are unknown
Symptoms including, insomnia, nausea, headache, anxiety, and diarrhea were reported following
abrupt or rapid discontinuation of treatment; increased seizure frequency may occur in patients
with seizure disorders and have rapid discontinued treatment; taper pregabalin gradually over a
minimum of 1 week rather than discontinuing the drug abruptly
In controlled studies, blurred vision and other vision-related events were reported with treatment;
clinical significance of the ophthalmologic findings is unknown, inform patients to notify their
physician if changes in vision occur; if visual disturbance persists, consider further assessment
Creatine kinase elevations has been associated with treatment; monitor for symptoms (eg,
unexplained muscle pain, tenderness, or weakness, particularly if these muscle symptoms are
accompanied by malaise or fever); discontinue treatment if myopathy is diagnosed or suspected
or if markedly elevated creatine kinase levels occur
Serious, life-threatening, or fatal respiratory depression reported when coadministered with
central nervous system depressants, including opioids, or in the setting of underlying respiratory
impairment; consider initiating therapy at low dose and monitor for symptoms of respiratory
depression and sedation if co-prescribing of another CNS depressant, like opioid, or prescribing
to patients with underlying respiratory impairment
Antiepileptic drugs increase risk of suicidal thoughts or behavior in patients taking these
drugs for any indication; monitor for emergence or worsening of depression, suicidal
thoughts or behavior, and/or any unusual changes in mood or behavior
Inform patients, their caregivers, and families of the increase the risk of suicidal thoughts
and behavior; advise to be alert for the emergence or worsening of signs and symptoms
Angioedema
Angioedema of the face, extremities, lips, tongue, glottis, and larynx has been reported
during initial and chronic treatment, including reports of life-threatening angioedema
with respiratory compromise requiring emergency intervention
If laryngeal stridor or angioedema of the face, tongue, or glottis occurs, discontinue
therapy and institute appropriate therapy immediately
Coadministration of ACE inhibitors or mTOR (mammalian target of rapamycin)
inhibitors (eg, temsirolimus, sirolimus, everolimus), or previous history of angioedema
may increase risk
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There are no adequate and well-controlled studies with pregabalin in pregnant women
Animal data
In the animal fertility study with pregabalin in male rats, adverse reproductive and
developmental effects were observed
In animal reproduction studies, increased incidences of fetal structural abnormalities and
other manifestations of developmental toxicity, including skeletal malformations,
retarded ossification, and decreased fetal body weight were observed in the offspring of
rats and rabbits given pregabalin orally during organogenesis, at doses that produced
plasma pregabalin exposures (AUC) greater than or equal to 16 times human exposure at
the maximum recommended dose (MRD) of 600 mg/day
Pregnancy Registry
Lactation
Small amounts of pregabalin have been detected in the milk of lactating women
Based on animal studies, there is a potential risk of tumorigenicity with pregabalin exposure via
breast milk to the breastfed infant
Available clinical study data in patients greater than 12 years of age do not provide a clear
conclusion about the potential risk of tumorigenicity with pregabalin
Pregnancy Categories
A: Generally acceptable. Controlled studies in pregnant women show no evidence of fetal risk.
B: May be acceptable. Either animal studies show no risk but human studies not available or
animal studies showed minor risks and human studies done and showed no risk.
C: Use with caution if benefits outweigh risks. Animal studies show risk and human studies not
available or neither animal nor human studies done.
D: Use in LIFE-THREATENING emergencies when no safer drug available. Positive evidence
of human fetal risk.
X: Do not use in pregnancy. Risks involved outweigh potential benefits. Safer alternatives exist.
NA: Information not available.
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Pharmacology
Mechanism of Action
Precise mechanism of action unknown but is a GABA analogue that binds to a subunit of
voltage-gated calcium channels in CNS; does not affect sodium channels, opiate receptors, or
cyclo-oxygenase enzyme activity; interactions with descending noradrenergic and serotonergic
pathways originating from the brain stem appear to reduce neuropathic pain transmission from
spinal cord
Absorption
Bioavailability: >90%
AUC (24 hr): 31.5 mcg·h/mL (75 mg capsule BID); 29.4 mcg·h/mL (165 mg ER tablet)
Peak plasma concentration: 3.2 mcg/mL (75 mg capsule BID); 2 mcg/mL (165 mg ER tablet)
Distribution
Although there are no data in humans, pregabalin has been shown to cross the blood brain barrier
in mice, rats, and monkeys
Metabolism
Minimal
Elimination
Half-life: 6.3 hr
Excretion: Urine
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Administration
Oral Administration
Capsules/oral solution
ER tablets
Storage
Store at 20-25°C (68-77°F), excursions permitted between 15-30°C (between 59-86°F) in the
original package
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Images
BRAND FORM. UNIT PRICEPILL IMAGE
Lyrica oral
25 mg capsule
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Lyrica oral
150 mg capsule
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Lyrica oral
300 mg capsule
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Lyrica oral
50 mg capsule
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Lyrica oral
75 mg capsule
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Lyrica oral
100 mg capsule
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Lyrica oral
200 mg capsule
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Lyrica oral
225 mg capsule
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Lyrica oral
20 mg/mL solution
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BRAND FORM. UNIT PRICEPILL IMAGE
pregabalin oral
225 mg capsule
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pregabalin oral
25 mg capsule
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pregabalin oral
150 mg capsule
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pregabalin oral
75 mg capsule
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pregabalin oral
50 mg capsule
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pregabalin oral
300 mg capsule
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pregabalin oral
225 mg capsule
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pregabalin oral
200 mg capsule
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pregabalin oral
150 mg capsule
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pregabalin oral
75 mg capsule
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pregabalin oral
50 mg capsule
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pregabalin oral
25 mg capsule
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pregabalin oral
300 mg capsule
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pregabalin oral
225 mg capsule
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pregabalin oral
200 mg capsule
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pregabalin oral
150 mg capsule
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pregabalin oral
100 mg capsule
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pregabalin oral
300 mg capsule
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pregabalin oral
225 mg capsule
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pregabalin oral
200 mg capsule
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pregabalin oral
150 mg capsule
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pregabalin oral
100 mg capsule
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pregabalin oral75 mg capsule
BRAND FORM. UNIT PRICEPILL IMAGE
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pregabalin oral
50 mg capsule
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pregabalin oral
25 mg capsule
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pregabalin oral
100 mg capsule
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pregabalin oral
300 mg capsule
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pregabalin oral
200 mg capsule
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pregabalin oral
150 mg capsule
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pregabalin oral
100 mg capsule
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pregabalin oral
50 mg capsule
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pregabalin oral
25 mg capsule
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pregabalin oral
75 mg capsule
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pregabalin oral
75 mg capsule
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pregabalin oral
50 mg capsule
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pregabalin oral
25 mg capsule
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pregabalin oral
150 mg capsule
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pregabalin oral
200 mg capsule
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pregabalin oral
100 mg capsule
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pregabalin oral
75 mg capsule
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pregabalin oral
50 mg capsule
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pregabalin oral
300 mg capsule
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pregabalin oral
150 mg capsule
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pregabalin oral
75 mg capsule
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pregabalin oral
25 mg capsule
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BRAND FORM. UNIT PRICEPILL IMAGE
pregabalin oral
100 mg capsule
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pregabalin oral
200 mg capsule
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pregabalin oral
225 mg capsule
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pregabalin oral
225 mg capsule
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pregabalin oral
150 mg capsule
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pregabalin oral
300 mg capsule
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pregabalin oral
100 mg capsule
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pregabalin oral
50 mg capsule
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pregabalin oral
25 mg capsule
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pregabalin oral
200 mg capsule
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pregabalin oral
25 mg capsule
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pregabalin oral
225 mg capsule
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pregabalin oral
300 mg capsule
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pregabalin oral
300 mg capsule
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pregabalin oral
150 mg capsule
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pregabalin oral
50 mg capsule
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pregabalin oral
225 mg capsule
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pregabalin oral
200 mg capsule
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pregabalin oral
100 mg capsule
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pregabalin oral
75 mg capsule
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pregabalin oral
200 mg capsule
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pregabalin oral
300 mg capsule
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pregabalin oral150 mg capsule
BRAND FORM. UNIT PRICEPILL IMAGE
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pregabalin oral
75 mg capsule
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pregabalin oral
100 mg capsule
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pregabalin oral
25 mg capsule
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pregabalin oral
225 mg capsule
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pregabalin oral
200 mg capsule
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pregabalin oral
300 mg capsule
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pregabalin oral
50 mg capsule
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pregabalin oral
75 mg capsule
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pregabalin oral
100 mg capsule
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pregabalin oral
50 mg capsule
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Patient Handout
Print
Patient Education
pregabalin oral
(pree-GAB-a-lin)
USES: This medication is used to treat pain caused by nerve damage due to diabetes or shingles
(herpes zoster) infection.
HOW TO USE: Read the Medication Guide provided by your pharmacist before you start taking
pregabalin and each time you get a refill. If you have any questions, ask your doctor or
pharmacist.Take this medication by mouth as directed by your doctor, usually once daily after an
evening meal. Swallow the tablets whole. Do not split, crush, or chew. Doing so can release all
of the drug at once, increasing the risk of side effects.The dosage is based on your medical
condition and response to treatment. To reduce your risk of side effects (such as dizziness and
drowsiness), your doctor may direct you to start this medication at a low dose and gradually
increase your dose. Follow your doctor's instructions carefully.Use this medication regularly to
get the most benefit from it. To help you remember, take it at the same time each day.Do not stop
taking this medication without consulting your doctor. Some conditions may become worse
when this drug is suddenly stopped. Also, you may experience symptoms such as difficulty
sleeping, nausea, headache, and diarrhea. To prevent these symptoms while you are stopping
treatment with this drug, your doctor may reduce your dose gradually. Report any new or
worsening symptoms right away.Though it helps many people, this medication may sometimes
cause addiction. This risk may be higher if you have a substance use disorder (such as overuse of
or addiction to drugs/alcohol). Take this medication exactly as prescribed to lower the risk of
addiction. Ask your doctor or pharmacist for more details.Tell your doctor if your condition lasts
or gets worse.
SIDE EFFECTS: Drowsiness, dizziness, headache, dry mouth, nausea, constipation, and weight
gain may occur. If any of these effects last or get worse, tell your doctor or pharmacist
promptly.Remember that this medication has been prescribed because your doctor has judged
that the benefit to you is greater than the risk of side effects. Many people using this medication
do not have serious side effects.Tell your doctor right away if you have any serious side effects,
including: vision changes (such as blurred vision), unusual bleeding/bruising, muscle
pain/tenderness/weakness (especially with fever or unusual tiredness), swelling
hands/ankles/feet.A small number of people who take anticonvulsants for any condition (such as
seizure, bipolar disorder, pain) may experience depression, suicidal thoughts/attempts, or other
mental/mood problems. Tell your doctor right away if you or your family/caregiver notice any
unusual/sudden changes in your mood, thoughts, or behavior such as signs of depression,
suicidal thoughts/attempts, thoughts about harming yourself.Get medical help right away if you
have any very serious side effects, including: slow/shallow breathing.A very serious allergic
reaction to this drug is rare. However, get medical help right away if you notice any symptoms of
a serious allergic reaction, including: rash, itching/swelling (especially of the face/tongue/throat),
severe dizziness, trouble breathing.This is not a complete list of possible side effects. If you
notice other effects not listed above, contact your doctor or pharmacist.In the US -Call your
doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-
1088 or at www.fda.gov/medwatch.In Canada - Call your doctor for medical advice about side
effects. You may report side effects to Health Canada at 1-866-234-2345.
PRECAUTIONS: Before taking pregabalin, tell your doctor or pharmacist if you are allergic to
it; or if you have any other allergies. This product may contain inactive ingredients, which can
cause allergic reactions or other problems. Talk to your pharmacist for more details.Before using
this medication, tell your doctor or pharmacist your medical history, especially of: heart
problems (such as heart failure), kidney disease, history of an allergic reaction which included
itching/swelling of the face/lips/tongue/throat (angioedema), personal or family history of a
substance use disorder (such as overuse of or addiction to drugs/alcohol), breathing problems
(such as COPD).This drug may make you dizzy or drowsy or cause blurred vision. Alcohol or
marijuana (cannabis) can make you more dizzy or drowsy. Do not drive, use machinery, or do
anything that needs alertness or clear vision until you can do it safely. Avoid alcoholic
beverages. Talk to your doctor if you are using marijuana (cannabis).Before having surgery, tell
your doctor or dentist about all the products you use (including prescription drugs,
nonprescription drugs, and herbal products).Older adults may be more sensitive to the side
effects of this drug, especially slow/shallow breathing.During pregnancy, this medication should
be used only when clearly needed. Discuss the risks and benefits with your doctor.This drug
passes into breast milk. Consult your doctor before breast-feeding.
DRUG INTERACTIONS: Drug interactions may change how your medications work or increase
your risk for serious side effects. This document does not contain all possible drug interactions.
Keep a list of all the products you use (including prescription/nonprescription drugs and herbal
products) and share it with your doctor and pharmacist. Do not start, stop, or change the dosage
of any medicines without your doctor's approval.A product that may interact with this drug is:
orlistat.The risk of serious side effects (such as slow/shallow breathing, severe
drowsiness/dizziness) may be increased if this medication is taken with other products that may
also cause drowsiness or breathing problems. Tell your doctor or pharmacist if you are using
other products such as opioid pain or cough relievers (such as codeine, hydrocodone), alcohol,
marijuana (cannabis), drugs for sleep or anxiety (such as alprazolam, lorazepam, zolpidem),
muscle relaxants (such as carisoprodol, cyclobenzaprine), or antihistamines (such as cetirizine,
diphenhydramine).Check the labels on all your medicines (such as allergy or cough-and-cold
products) because they may contain ingredients that cause drowsiness. Ask your pharmacist
about using those products safely.
OVERDOSE: If someone has overdosed and has serious symptoms such as passing out or
trouble breathing, call 911. Otherwise, call a poison control center right away. US residents can
call their local poison control center at 1-800-222-1222. Canada residents can call a provincial
poison control center.
NOTES: Do not share this medication with others. Sharing it is against the law.Lab and/or
medical tests (such as kidney function, platelet count) may be done while you are taking this
medication. Keep all medical and lab appointments. Consult your doctor for more details.
MISSED DOSE: If you miss a dose and remember before bedtime, take it after a snack before
bedtime. If it is the next morning when you remember, take the dose after the morning meal. If
you remember after the morning, skip the missed dose. Take your next dose at the regular time.
Do not double the dose to catch up.
STORAGE: Store at room temperature away from light and moisture. Do not store in the
bathroom. Keep all medications away from children and pets.Do not flush medications down the
toilet or pour them into a drain unless instructed to do so. Properly discard this product when it is
expired or no longer needed. Consult your pharmacist or local waste disposal company.
Information last revised August 2021. Copyright(c) 2021 First Databank, Inc.
IMPORTANT: HOW TO USE THIS INFORMATION: This is a summary and does NOT have
all possible information about this product. This information does not assure that this product is
safe, effective, or appropriate for you. This information is not individual medical advice and does
not substitute for the advice of your health care professional. Always ask your health care
professional for complete information about this product and your specific health needs.
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Formulary
FormularyPatient Discounts
Adding plans allows you to compare formulary status to other drugs in the same class.
To view formulary information first create a list of plans. Your list will be saved and can be
edited at any time.
The above information is provided for general informational and educational purposes
only. Individual plans may vary and formulary information changes. Contact the
applicable plan provider for the most current information.