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What the label lists and what reports show

Fish oil, medium-chain triglycerides, olive oil and soybean oil side effects

Fish oil, medium-chain triglycerides, olive oil and soybean oil's FDA label: “Most common adverse drug reactions (≥5%) from clinical trials in adults were nausea, vomiting, and hyperglycemia.” FAERS holds 844 reports naming it through July 30, 2026; the reaction reported most often, leaving out the conditions it is used for, product-use terms and outcomes, is pyrexia (57 reports).

  • No generic listed

Check it at the source: the fish oil, medium-chain triglycerides, olive oil and soybean oil FDA label on DailyMed (effective August 15, 2025); the FDA FAERS public dashboard.

What does the label list?

From the label: adverse reactions

Most common adverse drug reactions (≥5%) from clinical trials in adults were nausea, vomiting, and hyperglycemia.

Table 3: Adverse Reactions in >1% of Pediatric Patients Treated with SMOFlipid

Adverse ReactionNumber of Patients in SMOFlipid Group (N=170)Number of Patients in Soybean Oil lipid emulsion Comparator Group (N=163)
Anemia30 (18%)33 (20%)
Vomiting16 (9%)16 (10%)
Gamma-glutamyltransferase increased10 (6%)12 (7%)
Nosocomial infection10 (6%)6 (4%)
Cholestasis7 (4%)10 (6%)
Pyrexia7 (4%)7 (4%)
C-reactive protein increased6 (4%)7 (4%)
Hyperbilirubinemia5 (3%)7 (4%)
Abdominal pain4 (2%)5 (3%)
Bilirubin conjugated increased3 (2%)7 (4%)
Diarrhea3 (2%)4 (3%)
Tachycardia3 (2%)4 (3%)
Thrombocytopenia3 (2%)4 (3%)
Hyperglycemia3 (2%)2 (1%)
Sepsis3 (2%)2 (1%)

Rows and numbers as the label prints them, under its own column headings (the first rows of a longer table where it runs on). A reaction in a trial table is not necessarily caused by the medicine, and trials differ from everyday use.

From the label: adverse reactions, continued

Adverse reactions described elsewhere in this Prescribing Information are: • Clinical Decompensation with Rapid Infusion of Intravenous Lipid Emulsion in Neonates and Infants [see Warnings and Precautions ( 5.1 )] • Parenteral Nutrition-Associated Liver Disease and Other Hepatobiliary Disorders [see Warnings and Precautions ( 5.2 )] • Hypersensitivity Reactions [see Warnings and Precautions ( 5.3 )] • Infections [see Warnings and Precautions ( 5.4 )] • Fat Overload Syndrome [see Warnings and Precautions ( 5.5 )] • Refeeding Syndrome [see Warnings and Precautions ( 5.6 )] • Hypertriglyceridemia [see Warnings and Precautions ( 5.7 )] • Aluminum Toxicity [see Warnings and Precautions ( 5.8 )] • Essential Fatty Acid Deficiency [see Warnings and Precautions ( 5.9 )] Most common adverse drug reactions (≥5%) from clinical trials in adults were nausea, vomiting, and hyperglycemia. Most common adverse drug reactions (≥5%) from clinical trials in pediatric patients were anemia, vomiting, increased gamma-glutamyltransferase, and nosocomial infection. ( 6.1 ) To report SUSPECTED ADVERSE REACTIONS, contact Fresenius Kabi USA, LLC at 1-800-551-7176 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. …

Source: FDA drug label, Fresenius Kabi USA, LLC, effective August 15, 2025 (SPL set e0e9d917-ff6f-488e-a6a8-0ad59dd17d80), via openFDA; the full label on DailyMed

What do FAERS reports show?

844 reports list fish oil, medium-chain triglycerides, olive oil and soybean oil among the medicines taken, each a report of something that happened, not proof the medicine caused it; 101 are coded as a death and 338 as a hospital stay. Counts follow how widely a medicine is used and watched, and they are not a measure of how risky it is. Of the 21 reactions below, 16 are named by the same term (in US spelling) in the label's adverse reactions, warnings or patient leaflet; a reaction the label does not name may still be there under another word, and a report does not show that the medicine caused it.

Reports received each year

The 25 most reported reactions

  • Pyrexia (named in the label)57
  • Off Label Use (a use or a product term, not a reaction)51
  • Vomiting (named in the label)48
  • Nausea (named in the label)47
  • Malaise (named in the label)39
  • Dyspnoea (named in the label)37
  • Death (an outcome recorded in the report)36
  • Intentional Product Use Issue (a use or a product term, not a reaction)34
  • Fatty Acid Deficiency (named in the label)31
  • Hypertriglyceridaemia (named in the label)31
  • Chills (named in the label)30
  • Diarrhoea (named in the label)28
  • Cholestasis (named in the label)27
  • Parenteral Nutrition Associated Liver Disease (named in the label)25
  • Product Use Issue (a use or a product term, not a reaction)25
  • Sepsis (named in the label)25
  • Pain19
  • Rash (named in the label)18
  • Blood Triglycerides Increased (named in the label)17
  • Hypoglycaemia17
  • Vascular Device Infection17
  • Pruritus (named in the label)16
  • Weight Decreased16
  • Device Related Infection (named in the label)15
  • Drug Intolerance15

Source: FDA Adverse Event Reporting System (FAERS) via openFDA, reports through July 30, 2026; reactions as MedDRA preferred terms

What next?

Side effects hub
the most reported medicines and reactions