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Gladem adverse events reported to FDA.

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Summary

FDA Adverse Reports: 7. View All

Gladem FDA safety alerts: No

Reported deaths: 3

Reported hospitalizations: 5

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

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6334721-0 | Hyponatraemia
on Aug 17, 2009 Female patient from UNITED STATES , 80 years of age, was treated with Gladem (View Usage). Patient experienced the following unwanted or unexpected effects: hyponatraemia. Gladem dosage: 50 Mg, Unk. During the same period patient was treated with FUROHEXAL (40 Mg, 2x/day) (View Furohexal Review and Furohexal Label ), ASPIRIN (100 Mg, Ta) (View Aspirin Review and Aspirin Label ), CLYSMOL (View Clysmol Review and Clysmol Label ), BISOPROLOL FUMARATE (5 Mg, (1/2-0-0)) (View Bisoprolol Fumarate Review and Bisoprolol Fumarate Label ), DANCOR (10 Mg, 2x/day (1-0-1) Ta) (View Dancor Review and Dancor Label ), ENALAPRIL MALEATE (5 Mg, 2x/day (1/20-1/2) Ta) (View Enalapril Maleate Review and Enalapril Maleate Label ), EUTHYROX (75 Ug, Unk) (View Euthyrox Review and Euthyrox Label ), HALCION (0.25 Mg, Ta) (View Halcion Review and Halcion Label ). Patient was hospitalized.

5616007-2 | Dry Mouth, Muscle Spasms, Overdose, Pupil Fixed, Suicide Attempt, Tachycardia, Vomiting
Patient was taking Gladem (View Usage). Patient had the following side effects: dry mouth, muscle spasms, overdose, pupil fixed, suicide attempt, tachycardia, vomiting on Jan 31, 2008 from GERMANY Additional patient health information: Female patient , weighting 154.3 lb, . Gladem dosage: . Patient was hospitalized.

5590699-9 | Dizziness, Initial Insomnia, Myalgia, Somnolence
Adverse event was reported on Jan 08, 2008 by a Female patient taking Gladem (View Usage) (Dosage: Daily Dose:50mg) was diagnosed with somatoform disorder and. Location: AUSTRIA , 61 years of age, After Gladem was administered, patient had the following side effects: dizziness (What is dizziness?), initial insomnia, myalgia, somnolence. During the same period patient was treated with XANOR (Daily Dose:.75mg) (View Xanor Review and Xanor Label ), REMERON (Daily Dose:15mg) (View Remeron Review and Remeron Label ), PANTOLOC ^BYK^ (Daily Dose:20mg) (View Pantoloc ^byk^ Review and Pantoloc ^byk^ Label ), RESPICUR SLOW RELEASE (View Respicur - Slow Release Review and Respicur - Slow Release Label ), SPIRIVA (Daily Dose:18mcg) (View Spiriva Review and Spiriva Label ), CONCOR COR (Daily Dose:5mg) (View Concor Cor Review and Concor Cor Label ), OXIS (View Oxis Review and Oxis Label ), PULMICORT (View Pulmicort Review and Pulmicort Label ). Patient was hospitalized.

5411497-2 | Dizziness, Initial Insomnia, Myalgia, Somnolence
on Jul 31, 2007 Female patient from AUSTRIA , 61 years of age, was diagnosed with somatoform disorder and was treated with Gladem (View Usage). Patient experienced the following unwanted or unexpected effects: dizziness (What is dizziness?), initial insomnia, myalgia, somnolence. Gladem dosage: Daily Dose:50mg. During the same period patient was treated with XANOR (Daily Dose:.75mg) (View Xanor Review and Xanor Label ), REMERON (Daily Dose:15mg) (View Remeron Review and Remeron Label ), PANTOLOC ^BYK^ (Daily Dose:20mg) (View Pantoloc ^byk^ Review and Pantoloc ^byk^ Label ), RESPICUR SLOW RELEASE (View Respicur - Slow Release Review and Respicur - Slow Release Label ), SPIRIVA ^PFIZER^ (View Spiriva ^pfizer^ Review and Spiriva ^pfizer^ Label ), CONCOR COR (View Concor Cor Review and Concor Cor Label ), OXIS (View Oxis Review and Oxis Label ), PULMICORT (View Pulmicort Review and Pulmicort Label ). Patient was hospitalized.


5354669-8 | Hypotension, Overdose, Respiratory Depression, Somnolence, Suicide Attempt, Tachycardia
on Jun 04, 2007 Female patient from GERMANY , weighting 176.4 lb, was treated with Gladem (View Usage). Patient had the following side effects: hypotension, overdose, respiratory depression, somnolence, suicide attempt, tachycardia. Gladem dosage: . During the same period patient was treated with TAVOR (View Tavor Review and Tavor Label ).

5330393-2 | Hypotension, Overdose, Somnolence, Suicide Attempt, Tachycardia
Patient was taking Gladem (View Usage). After Gladem was administered, patient had the following side effects: hypotension, overdose, somnolence, suicide attempt, tachycardia on May 16, 2007 from GERMANY Additional patient health information: Female patient , weighting 176.4 lb, . Gladem dosage: . During the same period patient was treated with LORAZEPAM (View Lorazepam Review and Lorazepam Label ).

5114217-4 | Accidental Overdose
Adverse event was reported on Sep 19, 2006 by a Female patient taking Gladem (View Usage) (Dosage: ) . Location: GERMANY , weighting 24.25 lb, Patient experienced the following unwanted or unexpected effects: accidental overdose. 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 Gladem 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 Gladem quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Gladem 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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Gladem Reactions
Accidental Overdose
DizzinessWhat is Dizziness?
Dry Mouth
Hyponatraemia
Hypotension
Initial Insomnia
Muscle Spasms
Myalgia
Overdose
Pupil Fixed
Respiratory Depression
Somnolence
Suicide Attempt
Tachycardia
Vomiting
Gladem 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 Gladem 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!