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Aremis adverse events reported to FDA.

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Summary

FDA Adverse Reports: 3. View All

Aremis FDA safety alerts: No

Reported hospitalizations: 2

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

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5942435-1 | Hyponatraemia
on Oct 27, 2008 Female patient from SPAIN , 36 years of age, was diagnosed with depression (What is depression?), hypopituitarism and was treated with Aremis (View Usage). Patient experienced the following unwanted or unexpected effects: hyponatraemia. Aremis dosage: . During the same period patient was treated with DESMOPRESSIN ACETATE (View Desmopressin Acetate Review and Desmopressin Acetate Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), HYDROCORTISONE (View Hydrocortisone Review and Hydrocortisone Label ), ALPRAZOLAM (View Alprazolam Review and Alprazolam Label ). Patient was hospitalized.

5533471-8 | Gastrointestinal Haemorrhage
Patient was taking Aremis (View Usage). Patient had the following side effects: gastrointestinal haemorrhage on Nov 23, 2007 from SPAIN Additional patient health information: Female patient , 86 years of age, was diagnosed with depression (What is depression?), pain (What is pain?), angina pectoris, hypertension, insomnia, gastrooesophageal reflux prophylaxis and. Aremis dosage: . During the same period patient was treated with IBUPROFEN (View Ibuprofen Review and Ibuprofen Label ), MANIDON SLOW RELEASE (Text:120mg-freq:daily) (View Manidon - Slow Release Review and Manidon - Slow Release Label ), HIDROSALURETIL (Text:50mg-freq:daily) (View Hidrosaluretil Review and Hidrosaluretil Label ), ORFIDAL (Text:1mg-freq:daily) (View Orfidal Review and Orfidal Label ), OMEPRAZOLE (Text:20mg-freq:daily) (View Omeprazole Review and Omeprazole Label ). Patient was hospitalized.

5488765-1 | Hepatitis, Hepatocellular Damage
Adverse event was reported on Oct 05, 2007 by a Male patient taking Aremis (View Usage) (Dosage: ) was diagnosed with gastroenteritis (What is gastroenteritis?) and. Location: SPAIN , 52 years of age, After Aremis was administered, patient had the following side effects: hepatitis (What is hepatitis?), hepatocellular damage. During the same period patient was treated with TIORFAN (View Tiorfan Review and Tiorfan 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 Aremis 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 Aremis quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Aremis 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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Aremis Reactions
Gastrointestinal Haemorrhage
HepatitisWhat is Hepatitis?
Hepatocellular Damage
Hyponatraemia
Aremis 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 Aremis 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!