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Lactomin Side Effects

Common Lactomin Side Effects

The most commonly reported Lactomin side effects (click to view or check a box to report):

Rash (2)
Renal Impairment (2)
Alopecia (2)
Cholelithiasis (1)
Hyperkalaemia (1)
Skin Exfoliation (1)
No Adverse Event (1)
Anaemia (1)
Neutrophil Count Decreased (1)
Renal Disorder (1)
Papule (1)
Overdose (1)
Platelet Count Decreased (1)
Pruritus (1)
White Blood Cell Count Decreased (1)
Abdominal Pain (1)


If you or someone in your family has experienced a serious side effect to a health product, you are encouraged to report the experience to your health care professional (e.g. physician, pharmacist). You could also complete a copy of the side effect reporting form or report your side effect to FDA.

Side effects reports are analyzed to discover potential health product safety signals. Some important reactions may take an extremely long time to develop or occur infrequently. Continued monitoring of adverse reactions is thus essential to maintain a comprehensive safety and effectiveness profile of health products.

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).
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 found 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
  • Tamiflu
  • Periactin (Dosage Is Uncertain.)


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 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
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.

Keep Track of Side Effects

Note Your Observations

It is really important to keep of your symptoms, right from the time you start a new medicine. You can do it any way you prefer: in a notebook, in a computer file or using our online tool. You should also note down any other medicines you are taking at the same time, because there could be an interaction between these medicines.

Why Your Notes are Important

Your notes could be helpful in several ways:

  • You can use them to remind you of details that may alert your health care professional(s) to a problem
  • You will have a record to refer to in the future, in case you are ever prescribed the same medicine again

  • Log Form

    You can use the following log form to write down important information, like the date and time you experienced a side effect and your symptoms, how strong the symptoms were, and any other medicines you were using.

    Medicine Name and Dosage:

     

    Side Effects

    Scale

    Date & Time

    Other Medicine(s) or Treatment(s)

     

     

     

     

    Scale: 1 = very mild to 10 = very bad


    Track Online

  • User Sign In
  • Register to track your side effects

  • 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.

    Discuss Lactomin Side Effects

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    How Effective is Lactomin for You?

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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

    Lactomin Reviews

    No reviews, be a first to report a side effect via side effect reporting form