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Foliamin adverse events reported to FDA.

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Summary

FDA Adverse Reports: 1. View All

Foliamin FDA safety alerts: No

Reported deaths: 1

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

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4683950-0 | Blood Urine Present, Renal Failure Chronic
on Apr 07, 2005 Female patient from , 87 years of age, weighting 59.52 lb, was diagnosed with anaemia, nephrogenic anaemia, inflammation, pneumonia (What is pneumonia?), clostridium colitis and was treated with Foliamin (View Usage). Patient experienced the following unwanted or unexpected effects: blood urine present, renal failure chronic. Foliamin dosage: . During the same period patient was treated with EPOGIN (View Epogin Review and Epogin Label ), PRIMAXIN (View Primaxin Review and Primaxin Label ), FLAGYL (View Flagyl Review and Flagyl 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 Foliamin 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 Foliamin quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Foliamin 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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How Did You Deal with Side Effects?

... Sodium Review and Methotrexate Sodium Label ), SPLENDIL (Unk) (View Splendil Review and Splendil Label ), SLOW K (Unk) (View Slow-k Review and Slow-k Label ), FOLIAMIN (Unk ...

Myslee Label ), FOLIAMIN (Unk) (View Foliamin Review and Foliamin Label ), NOCBIN (Unk) (View Nocbin Review and Nocbin Label ), MIYA BM (Unk) (View Miya-bm Review and ...

... Methotrexate Review and Methotrexate Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ), FOLIAMIN (View Foliamin Review and Foliamin Label ), NEOISCOTIN ...

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... Methotrexate Label ), NSAIDS (View Nsaids Review and Nsaids Label ), BUCILLAMINE (View Bucillamine Review and Bucillamine Label ), FOLIAMIN (View Foliamin Review and Foliamin ...

... 00113801/ Review and Rheumatrex /00113801/ Label ), LORCAM (View Lorcam Review and Lorcam Label ), FOLIAMIN (View Foliamin Review and Foliamin Label ...

... Hypen Review and Hypen Label ), GASTER (View Gaster Review and Gaster Label ), REMICADE (View Remicade Review and Remicade Label ), FOLIAMIN (View Foliamin Review and Foliamin ...

... Dose Form=tab) (View Cimetidine Review and Cimetidine Label ), MAGNESIUM OXIDE (660-990 Mg) (View Magnesium Oxide Review and Magnesium Oxide Label ), FOLIAMIN (View Foliamin ...

)During the same period patient was treated with BENET (Dose Not Provided) (View Benet Review and Benet Label ), FOLIAMIN (Dose Not Provided) (View Foliamin Review and ...

During the same period patient was treated with RHEUMATREX (View Rheumatrex Review and Rheumatrex Label ), FOLIAMIN (View Foliamin Review and Foliamin Label ), BENET (View ...

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Foliamin Reactions
Blood Urine Present
Renal Failure Chronic
Foliamin 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 Foliamin 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!