Ferrum Side Effects

If You had Ferrum side effect, You are not alone. Other patients reported side effects.

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Ferrum adverse events reported to FDA.

Have You Experienced unusual Ferrum symptoms? PatientsVille.com collects and analyzes Ferrum side effect and adverse reports submitted by Ferrum users, such as .

Summary

FDA Adverse Reports: 3. View All

Ferrum FDA safety alerts: 2009

Reported hospitalizations: 1

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

5977840-0 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Cholestasis, Hepatic Function Abnormal
on Nov 21, 2008 Male patient from JAPAN , weighting 151.5 lb, was diagnosed with iron deficiency anaemia, brain stem infarction, cerebellar infarction, cerebral infarction, prophylaxis against gastrointestinal ulcer and was treated with Ferrum (View Usage). Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, cholestasis, hepatic function abnormal. Ferrum dosage: 305 Mg. During the same period patient was treated with PLAVIX (75 Mg) (View Plavix Review and Plavix Label ), TAKEPRON (15 Mg) (View Takepron Review and Takepron Label ). Patient was hospitalized.

5446408-7 | Cholestasis, Condition Aggravated
Patient was taking Ferrum (View Usage). Patient had the following side effects: cholestasis, condition aggravated on Aug 28, 2007 from JAPAN Additional patient health information: Female patient , weighting 110.2 lb, was diagnosed with angina pectoris, reflux oesophagitis, hyperlipidaemia, prophylaxis, percutaneous coronary intervention and. Ferrum dosage: Unk. During the same period patient was treated with LANDEL (Unk) (View Landel Review and Landel Label ), METOPROLOL TARTRATE (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ), LANSOPRAZOLE (Unk) (View Lansoprazole Review and Lansoprazole Label ), SIGMART (Unk) (View Sigmart Review and Sigmart Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), LIPITOR (5 Mg) (View Lipitor Review and Lipitor Label ), TICLOPIDINE HCL (200 Mg) (View Ticlopidine Hcl Review and Ticlopidine Hcl Label ), PLAVIX (View Plavix Review and Plavix Label ).

5422468-4 | Cholestasis, Condition Aggravated
Adverse event was reported on Aug 10, 2007 by a Female patient taking Ferrum (View Usage) (Dosage: Unk) was diagnosed with angina pectoris, reflux oesophagitis, percutaneous coronary intervention and. Location: JAPAN , weighting 110.2 lb, After Ferrum was administered, patient had the following side effects: cholestasis, condition aggravated. During the same period patient was treated with LANDEL (Unk) (View Landel Review and Landel Label ), METOPROLOL TARTRATE (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ), LANSOPRAZOLE (Unk) (View Lansoprazole Review and Lansoprazole Label ), SIGMART (Unk) (View Sigmart Review and Sigmart Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), LIPITOR (5 Mg) (View Lipitor Review and Lipitor Label ), TICLOPIDINE HCL (200 Mg) (View Ticlopidine Hcl Review and Ticlopidine Hcl Label ), PLAVIX (View Plavix Review and Plavix Label ).

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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 Ferrum 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 Ferrum quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Ferrum 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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FERRUM Side Effects

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Ferrum adverse events reported to FDA.

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Ferrum Adverse Effect Reports (FDA)

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Ferrum Reactions

Alanine Aminotransferase Increased
Aspartate Aminotransferase Increased
Blood Alkaline Phosphatase Increased
Cholestasis
Condition Aggravated
Hepatic Function Abnormal

FERRUM Side Effects

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Detailed Reporting will help others get complete information and find alternative treatments to avoid or reduce side effects associated with it.

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Ferrum adverse events reported to FDA.

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Ferrum Adverse Effect Reports (FDA)

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Ferrum Reactions