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Lactomin Side Effects and Adverse Effects reported to US Food and Drug Administration (FDA)

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Renal Impairment, Alopecia, Rash (8304406-X)
on Apr 16, 2012 Female from JAPAN , weighting 105.8 lb, was diagnosed with
  • crohn's disease
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 (8274540-1)
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
  • Tamiflu
  • Periactin (Dosage Is Uncertain.)

Skin Exfoliation, Alopecia, Papule, Renal Impairment, Pruritus, Rash (8216078-3)
Adverse event was reported on Mar 09, 2012 by a Female taking Lactomin (Dosage: N/A) was diagnosed with
  • crohn's disease
  • postoperative care
  • systemic lupus erythematosus
  • dermatitis
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 (7798062-7)
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)
  • Humira
  • Mesalamine (300mg Daily)
  • Humira
Patient was hospitalized.

White Blood Cell Count Decreased, Hyperkalaemia, Anaemia, Neutrophil Count Decreased, Renal Disorder, Platelet Count Decreased (7737901-2)
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:
  • Sulfamethoxazole And Trimethoprim
  • Acyclovir
  • Granisetron Hydrochloride
  • Treanda
Patient was hospitalized.

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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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