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Micropakine adverse events reported to FDA.

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Summary

FDA Adverse Reports: 7. View All

Micropakine FDA safety alerts: No

Reported hospitalizations: 6

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Often additional risks of using a medication, such as Micropakine, become known after product is used by a larger number of patients, for a longer period of time, and by patients with different health characteristics from those studied before drug approval. This page allows You to Find answers and discuss health symptoms with other Micropakine users, Learn more about unwanted side effects & find ways to reduce them. Browse Micropakine Adverse Reports reported to FDA and participate in Micropakine discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Micropakine. You can also Post a question to users community or Ask a Doctor. PatientsVille.com is Your Complete Guide to all common, undocumented and undisclosed side effects associated with drugs and vaccines. Browse More Drug Reports Here: A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

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Micropakine Adverse Effect Reports (FDA)

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6725780-1 | Mouth Ulceration, Pruritus, Rash Maculo-papular, Toxic Skin Eruption
on May 07, 2010 Male patient from FRANCE , child 6 years of age, was diagnosed with epilepsy (What is epilepsy?), ear infection (What is ear infection?) and was treated with Micropakine (View Usage). Patient experienced the following unwanted or unexpected effects: mouth ulceration, pruritus, rash maculo-papular, toxic skin eruption. Micropakine dosage: Prolonged-release Granules. During the same period patient was treated with ROCEPHIN (View Rocephin Review and Rocephin Label ), NUREFLEX (View Nureflex Review and Nureflex Label ), PRODILANTIN (View Prodilantin Review and Prodilantin Label ), RIVOTRIL (View Rivotril Review and Rivotril Label ), URBANYL (View Urbanyl Review and Urbanyl Label ), TEGRETOL (View Tegretol Review and Tegretol Label ). Patient was hospitalized.

6066508-0 | Epilepsy, Liver Disorder
Patient was taking Micropakine (View Usage). Patient had the following side effects: epilepsy (What is epilepsy?), liver disorder on Jan 27, 2009 from FRANCE Additional patient health information: Female patient , 14 years of age, . Micropakine dosage: .

6063901-7 | Epilepsy, Treatment Noncompliance
Adverse event was reported on Jan 28, 2009 by a Male patient taking Micropakine (View Usage) (Dosage: ) was diagnosed with epilepsy (What is epilepsy?) and. Location: FRANCE , 19 years of age, After Micropakine was administered, patient had the following side effects: epilepsy (What is epilepsy?), treatment noncompliance. During the same period patient was treated with DEPAKENE (View Depakene Review and Depakene Label ).

6036324-4 | Epilepsy, Treatment Noncompliance
on Jan 07, 2009 Male patient from FRANCE , 19 years of age, was diagnosed with epilepsy (What is epilepsy?) and was treated with Micropakine (View Usage). Patient experienced the following unwanted or unexpected effects: epilepsy (What is epilepsy?), treatment noncompliance. Micropakine dosage: . During the same period patient was treated with DEPAKENE (View Depakene Review and Depakene Label ).


5537770-5 | Epilepsy
on Nov 28, 2007 Male patient from FRANCE , 16 years of age, was diagnosed with epilepsy (What is epilepsy?) and was treated with Micropakine (View Usage). Patient had the following side effects: epilepsy (What is epilepsy?). Micropakine dosage: . Patient was hospitalized.

5148864-0 | Klebsiella Infection, Myelodysplastic Syndrome, Pancytopenia, Pyrexia, Reticulocyte Count Increased, Unevaluable Event
Patient was taking Micropakine (View Usage). After Micropakine was administered, patient had the following side effects: klebsiella infection, myelodysplastic syndrome, pancytopenia, pyrexia, reticulocyte count increased, unevaluable event on Nov 02, 2006 from FRANCE Additional patient health information: Female patient , 71 years of age, . Micropakine dosage: . During the same period patient was treated with ESOMEPRAZOLE MAGNESIUM (View Esomeprazole Magnesium Review and Esomeprazole Magnesium Label ), ADRAFINIL (View Adrafinil Review and Adrafinil Label ), FLUINDIONE (View Fluindione Review and Fluindione Label ), PREDNISOLONE SODIUM PHOSPHATE (View Prednisolone Sodium Phosphate Review and Prednisolone Sodium Phosphate Label ), TIANEPTINE (View Tianeptine Review and Tianeptine Label ), ACENOCOUMAROL (View Acenocoumarol Review and Acenocoumarol Label ). Patient was hospitalized.

5148424-1 | Klebsiella Infection, Myelodysplastic Syndrome, Pancytopenia, Pyrexia, Reticulocyte Count Increased, Unevaluable Event
Adverse event was reported on Nov 02, 2006 by a Female patient taking Micropakine (View Usage) (Dosage: ) . Location: FRANCE , 71 years of age, Patient experienced the following unwanted or unexpected effects: klebsiella infection, myelodysplastic syndrome, pancytopenia, pyrexia, reticulocyte count increased, unevaluable event. During the same period patient was treated with ESOMEPRAZOLE MAGNESIUM (View Esomeprazole Magnesium Review and Esomeprazole Magnesium Label ), ADRAFINIL (View Adrafinil Review and Adrafinil Label ), FLUINDIONE (View Fluindione Review and Fluindione Label ), PREDNISOLONE SODIUM PHOSPHATE (View Prednisolone Sodium Phosphate Review and Prednisolone Sodium Phosphate Label ), TIANEPTINE (View Tianeptine Review and Tianeptine Label ), ACENOCOUMAROL (View Acenocoumarol Review and Acenocoumarol Label ). Patient was hospitalized.


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To find out about documented side effects or safety concerns read either the drug label or the drug's package insert. You may also want to speak with your pharmacist or healthcare provider. All medicines have benefits and risks. The risks are the chances that something unwanted or unexpected could happen to you when you use them. You can protect yourself by searching summaries of recent safety alerts, adverse reports. Sometimes there are risks that only come to light after a medical product gets on the market and is used in a larger number of patients, for a longer period of time, and in patients whose health characteristics are different from those of the patients studied before approval.

Be aware of the following potential Micropakine risks to be aware of: 1. Watch for any Serious adverse events, such as life-threatening situation, which can require an admission to hospital or longer-than-expected hospital stay, permanent disability, birth defect, miscarriage, stillbirth, or birth with serious disease requires medical care to prevent permanent damage
2. Any potential Micropakine quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Micropakine use error: mixing up products with similar drug names or packaging, taking wrong dose of a drug because of confusing dosing instructions on label
4. When applicable, Problems with different manufacturer of same medicine: not getting same results from a generic drug as a brand name drug, or from another generic

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Micropakine Reactions
EpilepsyWhat is Epilepsy?
Klebsiella Infection
Liver Disorder
Mouth Ulceration
Myelodysplastic Syndrome
Pancytopenia
Pruritus
Pyrexia
Rash Maculo-papular
Reticulocyte Count Increased
Toxic Skin Eruption
Treatment Noncompliance
Unevaluable Event
Micropakine Side Effects Notice - The material on this site is for informational purposes only, and is not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. PatientsVille.com does not provide medical advice, diagnosis or treatment. The information regarding Micropakine adverse reports, reviews and polls contained on PatientsVille.com site has not been scientifically or otherwise verified as to a cause and effect relationship and cannot be used to estimate the incidence of adverse drug reactions or for establishing or changing of patient treatments. Thank you for visiting Patientsville.com!