Pitavastatin adverse reactions: Difference between revisions

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#REDIRECT [[Pitavastatin#Adverse Reactions]]
{{Pitavastatin}}
{{CMG}}; {{AE}} {{SS}}
 
==Adverse Reactions==
 
The following serious adverse reactions are discussed in greater detail in other sections of the label:
 
[[Rhabdomyolysis]] with [[myoglobinuria]] and [[acute renal failure]] and [[myopathy]] (including [[myositis]]) [see Warnings and Precautions (5.1)].
Liver Enzyme Abnormalities [see Warning and Precautions (5.2)].
 
Of 4,798 patients enrolled in 10 controlled clinical studies and 4 subsequent open-label extension studies, 3,291 patients were administered pitava[[statin]] 1 mg to 4 mg daily. The mean continuous exposure of pitava[[statin]] (1 mg to 4 mg) was 36.7 weeks (median 51.1 weeks). The mean age of the patients was 60.9 years (range; 18 years – 89 years) and the gender distribution was 48% males and 52% females. Approximately 93% of the patients were Caucasian, 7% were Asian/Indian, 0.2% were African American and 0.3% were Hispanic and other.
 
===Clinical Studies Experience===
 
Because clinical studies on LIVALO are conducted in varying study populations and study designs, the frequency of adverse reactions observed in the clinical studies of LIVALO cannot be directly compared with that in the clinical studies of other [[HMG-CoA]] reductase inhibitors and may not reflect the frequency of adverse reactions observed in clinical practice.
 
Adverse reactions reported in ≥ 2% of patients in controlled clinical studies and at a rate greater than or equal to placebo are shown in Table 1. These studies had treatment duration of up to 12 weeks.
 
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Other adverse reactions reported from clinical studies were [[arthralgia]], [[headache]], [[influenza]], and [[nasopharyngitis]].
 
The following laboratory abnormalities have also been reported: elevated creatine phosphokinase, transaminases, alkaline phosphatase, bilirubin, and glucose.
 
In controlled clinical studies and their open-label extensions, 3.9% (1 mg), 3.3% (2 mg), and 3.7% (4 mg) of pitava[[statin]]-treated patients were discontinued due to adverse reactions. The most common adverse reactions that led to treatment discontinuation were: elevated creatine phosphokinase (0.6% on 4 mg) and myalgia (0.5% on 4 mg).
 
Hypersensitivity reactions including [[rash]], [[pruritus]], and [[urticaria]] have been reported with LIVALO.
 
===Postmarketing Experience===
 
The following adverse reactions have been identified during postapproval use of LIVALO. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.
 
Adverse reactions associated with LIVALO therapy reported since market introduction, regardless of causality assessment, include the following: abdominal discomfort, abdominal pain, [[dyspepsia]], [[nausea]], [[asthenia]], [[fatigue]], [[malaise]], [[hepatitis]], [[jaundice]], fatal and non-fatal hepatic failure, [[dizziness]], [[hypoesthesia]], [[insomnia]], [[depression]], interstitial lung disease, [[erectile dysfunction]] and [[muscle spasm]]s.
 
There have been rare postmarketing reports of cognitive impairment (e.g., memory loss, forgetfulness, [[amnesia]], memory impairment, confusion) associated with [[statin]] use. These cognitive issues have been reported for all [[statin]]s. The reports are generally nonserious, and reversible upon [[statin]] discontinuation, with variable times to symptom onset (1 day to years) and symptom resolution (median of 3 weeks).
 
There have been rare reports of immune-mediated necrotizing myopathy associated with [[statin]] use [see Warnings and Precautions (5.1)].<ref name="dailymed.nlm.nih.gov">{{Cite web  | last =  | first =  | title = LIVALO (PITAVA[[statin]] CALCIUM) TABLET, FILM COATED [KOWA PHARMACEUTICALS AMERICA, INC. ] | url = http://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=44dcbf97-99ec-427c-ba50-207e0069d6d2 | publisher =  | date =  | accessdate = 14 February 2014 }}</ref>
 
 
==References==
{{Reflist|2}}
 
{{[[statin]]s}}
 
[[Category:[[statin]]s]]
[[Category:Quinolines]]
[[Category:Diols]]
[[Category:Carboxylic acids]]
[[Category:Organofluorides]]
[[Category:Cyclopropanes]]
[[Category:Cardiovascular Drugs]]
[[Category:Drugs]]

Latest revision as of 00:39, 22 July 2014