Lactomin Side Effects

Report Lactomin Side Effects

If you experienced any harmful or unwanted effects of Lactomin, please share your experience. This could help to raise awareness about Lactomin side effects, identify uknown risks and inform health professionals and patients taking Lactomin.

Examples: headache, dizziness

Lactomin Side Effects reported to FDA

The following Lactomin reports list potential signals of serious risks and new safety information that were identified using the FDA Adverse Event Reporting System (FAERS).
The FAERS is a database that contains information on adverse event and medication errors reports submitted to FDA by healthcare professionals (such as physicians, pharmacists, nurses and others), consumers (such as patients, family members, layers and others) and manufacturers.

The appearance of Lactomin on this list does not mean that FDA has concluded that the drug has the listed risk. It means that FDA has identified a potential safety issue, but it does not mean that FDA has identified a causal relationship between the drug and the listed risk.

Renal Impairment, Alopecia, Rash
on Apr 16, 2012 Female from JAPAN , weighting 105.8 lb, was diagnosed with and was treated with Lactomin. Directly after, patient experienced the unwanted or unexpected Lactomin side effects: renal impairment, alopecia, rash. Lactomin dosage: N/A.
Associated medications used:
  • Ferrous Fumarate
  • Maltose/lactated Ringer's Solution
  • Dipyridamole
  • Antibiotics-resistant Lactic Acid Bacteriae
  • Sodium Bicarbonate/anyhydrous Monobasic Sodium Phosphate
  • Tribenoside/lidocaine
  • Famotidine
  • Famotidine

Overdose, No Adverse Event
Patient was taking Lactomin. Patient felt the following Lactomin side effects: overdose, no adverse event on Mar 10, 2012 from JAPAN Additional patient health information: Female , child 3 years of age, weighting 33.07 lb, . Lactomin dosage: Dosage Is Uncertain..
Multiple prescriptions taken:
  • Tamiflu (Dry Syrup 3%)
  • Methy-f (Dosage Is Uncertain.)
  • Albumin Tannate (Dosage Is Uncertain.)
  • Adsorbin (Dosage Is Uncertain.)
  • Mucosolvan (Dosage Is Uncertain.)
  • Sodium Azulene Sulfonate

Skin Exfoliation, Alopecia, Papule, Renal Impairment, Pruritus, Rash
Adverse event was reported on Mar 09, 2012 by a Female taking Lactomin (Dosage: N/A) was diagnosed with and. Location: JAPAN , weighting 105.8 lb, After Lactomin was administered, patient encountered several Lactomin side effects: skin exfoliation, alopecia, papule, renal impairment, pruritus, rash.
Multiple concurrent drugs taken:
  • Solita-t No.3
  • Candesartan Cilexetil
  • Azulene
  • Antibiotics-resistant Lactic Acid Bacteriae
  • Ferric Oxide Saccharated
  • Ascorbic Acid
  • Sennoside
  • Humira

Cholelithiasis, Abdominal Pain
on Oct 03, 2011 Male from JAPAN , weighting 167.6 lb, was diagnosed with
  • disbacteriosis
  • crohn's disease
  • diarrhoea
  • folate deficiency
  • gastrooesophageal reflux disease
and was treated with Lactomin. Directly after, patient experienced the unwanted or unexpected Lactomin side effects: cholelithiasis, abdominal pain. Lactomin dosage: 6 Gram Daily.
Associated medications used:
  • Humira
  • Natural Aluminun Silicate (3 Gram Daily)
  • Folic Acid (15 Mg Daily)
  • Omeprazole (20 Milligram)
  • Domperidone (30 Mg Daily)
Patient was hospitalized.

White Blood Cell Count Decreased, Hyperkalaemia, Anaemia, Neutrophil Count Decreased, Renal Disorder, Platelet Count Decreased
on Aug 11, 2011 Male from JAPAN , weighting 116.8 lb, was treated with Lactomin. Patient felt the following Lactomin side effects: white blood cell count decreased, hyperkalaemia, anaemia, neutrophil count decreased, renal disorder, platelet count decreased. Lactomin dosage: N/A.
Multiple prescriptions taken: Patient was hospitalized.

Record and Track Your Side Effects

It is very important to keep track of all side effects and discuss them with your doctor. If you think you may have a medical emergency, call your doctor or 911 immediately.

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Most drugs have a large list of nonsevere or mild adverse effects which do not rule out continued usage. These effects depend on individual sensitivity, and can include nausea, dizziness, diarrhea, malaise, vomiting, headache, dermatitis, dry mouth, etc. Check commonly reported side effects . These can be considered a form of pseudo-allergic reaction, as not all users experience these effects; many users experience none at all.

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.

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Safety Alerts, Active Ingredients, Usage Information

More About Lactomin

Side Effects reported to FDA: 5

Lactomin safety alerts: No

Reported hospitalizations: 2

Latest Lactomin clinical trials

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