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Fortimel adverse events reported to FDA.

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Summary

FDA Adverse Reports: 3. View All

Fortimel FDA safety alerts: No

Reported hospitalizations: 3

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Often additional risks of using a medication, such as Fortimel, 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 Fortimel users, Learn more about unwanted side effects & find ways to reduce them. Browse Fortimel Adverse Reports reported to FDA and participate in Fortimel discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Fortimel. 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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Fortimel Adverse Effect Reports (FDA)

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5367584-0 | Disorientation, Hyponatraemia, Subileus, Vomiting
on Oct 18, 2006 Female patient from FRANCE , 90 years of age, was treated with Fortimel (View Usage). Patient experienced the following unwanted or unexpected effects: disorientation, hyponatraemia, subileus, vomiting. Fortimel dosage: 1 Packet At 16:00. During the same period patient was treated with VASTAREL (View Vastarel Review and Vastarel Label ), LAXOMIL (View Laxomil Review and Laxomil Label ), INIPOMP (View Inipomp Review and Inipomp Label ), FORLAX (View Forlax Review and Forlax Label ), PAROXETINE HCL (View Paroxetine Hcl Review and Paroxetine Hcl Label ), AMLODIPINE (View Amlodipine Review and Amlodipine Label ), MODURETIC 5 50 (View Moduretic 5-50 Review and Moduretic 5-50 Label ), PLAVIX (View Plavix Review and Plavix Label ). Patient was hospitalized.

5138664-X | Disorientation, Hyponatraemia, Sigmoiditis, Subileus, Vomiting
Patient was taking Fortimel (View Usage). Patient had the following side effects: disorientation, hyponatraemia, sigmoiditis, subileus, vomiting on Oct 18, 2006 from FRANCE Additional patient health information: Female patient , 90 years of age, . Fortimel dosage: 1 Packet At 16:00. During the same period patient was treated with VASTAREL (View Vastarel Review and Vastarel Label ), LAXOMIL (View Laxomil Review and Laxomil Label ), INIPOMP (View Inipomp Review and Inipomp Label ), FORLAX (View Forlax Review and Forlax Label ), PAROXETINE HCL (View Paroxetine Hcl Review and Paroxetine Hcl Label ), AMLODIPINE (View Amlodipine Review and Amlodipine Label ), MODURETIC 5 50 (View Moduretic 5-50 Review and Moduretic 5-50 Label ), PLAVIX (View Plavix Review and Plavix Label ). Patient was hospitalized.

5138664-X | Disorientation, Hyponatraemia, Sigmoiditis, Subileus, Vomiting
Adverse event was reported on Oct 18, 2006 by a Female patient taking Fortimel (View Usage) (Dosage: 1 Packet At 16:00) . Location: FRANCE , 90 years of age, After Fortimel was administered, patient had the following side effects: disorientation, hyponatraemia, sigmoiditis, subileus, vomiting. During the same period patient was treated with VASTAREL (View Vastarel Review and Vastarel Label ), LAXOMIL (View Laxomil Review and Laxomil Label ), INIPOMP (View Inipomp Review and Inipomp Label ), FORLAX (View Forlax Review and Forlax Label ), DEROXAT (View Deroxat Review and Deroxat Label ), AMLOR (View Amlor Review and Amlor Label ), MODURETIC 5 50 (View Moduretic 5-50 Review and Moduretic 5-50 Label ), PLAVIX (View Plavix Review and Plavix 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 Fortimel 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 Fortimel quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Fortimel 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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During the same period patient was treated with SPIRONOLACTONE, MORPHINE (1-3 Times Per Day), FENTANYL CITRATE (As Used: 12 G), NULYTELY, FORTIMEL.

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Fortimel Reactions
Disorientation
Hyponatraemia
Sigmoiditis
Subileus
Vomiting
Fortimel 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 Fortimel 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!