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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

LEVOCARNITINE for Hyperammonaemia: Side Effects & Safety Data

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There are 13 adverse event reports in the FDA FAERS database where LEVOCARNITINE was used for Hyperammonaemia.

Most Reported Side Effects for LEVOCARNITINE

Side Effect Reports % Deaths Hosp.
Drug ineffective 54 13.8% 16 36
Fatigue 24 6.1% 0 17
Seizure 19 4.9% 0 8
Dyspnoea 18 4.6% 1 15
Nausea 17 4.3% 1 6
Status epilepticus 17 4.3% 0 15
Vomiting 17 4.3% 0 11
Off label use 16 4.1% 5 12
Hepatocellular injury 15 3.8% 0 5
Cardiac failure 12 3.1% 8 5
Blood alkaline phosphatase increased 11 2.8% 0 1
Blood bilirubin increased 11 2.8% 0 1
Cholestasis 11 2.8% 0 1
Condition aggravated 10 2.6% 3 8
Dyschromatopsia 10 2.6% 0 0

Other Indications for LEVOCARNITINE

Carnitine deficiency (97) Product used for unknown indication (85) Status epilepticus (12) Parenteral nutrition (11) Epilepsy (10) Methylmalonic aciduria (9) Seizure (9) Weight decreased (8) Hyperammonaemic encephalopathy (7)

Other Drugs Used for Hyperammonaemia

CARGLUMIC ACID (114) RIFAXIMIN (88) LACTULOSE (57) SODIUM\SODIUM PHENYLACETATE (16) GLYCEROL PHENYLBUTYRATE (14) SODIUM (13) SODIUM PHENYLBUTYRATE (13) ARGININE (12) ACARBOSE (5)

Related Pages

LEVOCARNITINE Full Profile All Hyperammonaemia Drugs LEVOCARNITINE Demographics LEVOCARNITINE Timeline