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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
This is a report of a female patient (weight: NA) from JAPAN, suffering from the following symptoms/conditions: crohn's disease, who was treated with Lactomin (dosage: NA, start time: Apr 27, 2011), combined with:
  • Ferrous Fumarate
  • Maltose/lactated Ringer's Solution
  • Dipyridamole
  • Antibiotics-resistant Lactic Acid Bacteriae
  • Sodium Bicarbonate/anyhydrous Monobasic Sodium Phosphate
  • Tribenoside/lidocaine
  • Famotidine
  • Famotidine
and developed a serious reaction and side effect(s). The consumer presented with:
  • Renal Impairment
  • Alopecia
  • Rash
which developed after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Lactomin treatment in female patients, resulting in renal impairment side effect.

Overdose, No Adverse Event
This report suggests a potential Lactomin Overdose, No Adverse Event side effect(s) that can have serious consequences. A 3-year-old female patient (weight: NA) from JAPAN was diagnosed with the following symptoms/conditions: NA and used Lactomin (dosage: Dosage Is Uncertain.) starting Mar 09, 2012. Soon after starting Lactomin the patient began experiencing various side effects, including:
  • Overdose
  • No Adverse Event
Drugs used concurrently:
  • 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.)
Although Lactomin demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as overdose, may still occur.

Skin Exfoliation, Alopecia, Papule, Renal Impairment, Pruritus, Rash
This Skin Exfoliation, Alopecia, Papule, Renal Impairment, Pruritus, Rash problem was reported by a physician from JAPAN. A female patient (weight: NA) was diagnosed with the following symptoms/conditions: crohn's disease,postoperative care,systemic lupus erythematosus,dermatitis. On Apr 28, 2011 this consumer started treatment with Lactomin (dosage: NA). The following drugs were being taken at the same time:
  • Solita-t No.3
  • Candesartan Cilexetil
  • Azulene
  • Antibiotics-resistant Lactic Acid Bacteriae
  • Ferric Oxide Saccharated
  • Ascorbic Acid
  • Sennoside
  • Humira
When commencing Lactomin, the patient experienced the following unwanted symptoms/side effects:
  • Skin Exfoliation
  • Alopecia
  • Papule
  • Renal Impairment
  • Pruritus
  • Rash
Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as skin exfoliation, may become evident only after a product is in use by the general population.

Cholelithiasis, Abdominal Pain
This is a report of a male patient (weight: NA) from JAPAN. The patient developed the following symptoms/conditions: disbacteriosis,crohn's disease,diarrhoea,folate deficiency,gastrooesophageal reflux disease and was treated with Lactomin (dosage: 6 Gram Daily) starting Mar 24, 2011. Concurrently used drugs:
  • Humira
  • Natural Aluminun Silicate (3 Gram Daily)
  • Folic Acid (15 Mg Daily)
  • Omeprazole (20 Milligram)
  • Domperidone (30 Mg Daily)
  • Humira
  • Mesalamine (300mg Daily)
  • Humira
Soon after that, the consumer experienced the following side effects:
  • Cholelithiasis
  • Abdominal Pain
The patient was hospitalized. This opens a possibility that Lactomin treatment could cause the above reactions, including cholelithiasis, and some male subjects may be more susceptible.


White Blood Cell Count Decreased, Hyperkalaemia, Anaemia, Neutrophil Count Decreased, Renal Disorder, Platelet Count Decreased
A male patient (weight: NA) from JAPAN with the following symptoms/conditions: NA started Lactomin treatment (dosage: NA) on Jan 13, 2011. Soon after starting Lactomin treatment, the subject experienced various side effects, including:
  • White Blood Cell Count Decreased
  • Hyperkalaemia
  • Anaemia
  • Neutrophil Count Decreased
  • Renal Disorder
  • Platelet Count Decreased
Concurrently used drugs:
  • Sulfamethoxazole And Trimethoprim
  • Acyclovir
  • Granisetron Hydrochloride
  • Treanda
The patient was hospitalized. This finding indicates that some male patients could be more vulnerable to Lactomin.



Top 10 Lactomin Side Effects for Women

Women Side EffectsReports
Alopecia 2
Rash 2
Renal Impairment 2
No Adverse Event 1
Overdose 1
Papule 1
Pruritus 1
Skin Exfoliation 1

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

    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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    Lactomin Safety Alerts, Active Ingredients, Usage Information

    More About Lactomin

    Side Effects reported to FDA: 5

    Lactomin safety alerts: No

    Reported hospitalizations: 2

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