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Depamide adverse events reported to FDA.

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Summary

FDA Adverse Reports: 5. View All

Depamide FDA safety alerts: No

Reported hospitalizations: 5

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

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5591020-2 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Cellulitis, Cytolytic Hepatitis, Haematology Test Abnormal, Tooth Infection
on Jan 07, 2008 Male patient from FRANCE , 29 years of age, was diagnosed with epilepsy (What is epilepsy?), aggression and was treated with Depamide (View Usage). Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, aspartate aminotransferase increased, cellulitis (What is cellulitis?), cytolytic hepatitis, haematology test abnormal, tooth infection. Depamide dosage: 600 Mg, Tid. During the same period patient was treated with ANDROCUR (100 Mg, Bid) (View Androcur Review and Androcur Label ), RIVOTRIL (4 Mg, Qd) (View Rivotril Review and Rivotril Label ), TAMSULOSIN HCL (0.4 Mg Per Day) (View Tamsulosin Hcl Review and Tamsulosin Hcl Label ), SEGLOR (5 Mg, Bid) (View Seglor Review and Seglor Label ), MESTINON (60 Mg, Qid) (View Mestinon Review and Mestinon Label ), LEPONEX (50 Mg Daily) (View Leponex Review and Leponex Label ). Patient was hospitalized.

5574562-5 | Caesarean Section, Maternal Hypertension Affecting Foetus, Oedema Peripheral, Pre-eclampsia, Vaginal Infection
Patient was taking Depamide (View Usage). Patient had the following side effects: caesarean section, maternal hypertension affecting foetus, oedema peripheral, pre-eclampsia, vaginal infection on Dec 17, 2007 from FRANCE Additional patient health information: Female patient , 36 years of age, . Depamide dosage: . During the same period patient was treated with ZOLOFT (Unk) (View Zoloft Review and Zoloft Label ), VALIUM (Unk) (View Valium Review and Valium Label ), STILNOX (View Stilnox Review and Stilnox Label ), TIAPRIDAL (Unk) (View Tiapridal Review and Tiapridal Label ). Patient was hospitalized.

5354512-7 | Maternal Hypertension Affecting Foetus, Oedema Peripheral, Pre-eclampsia, Vaginal Infection
Adverse event was reported on May 31, 2007 by a Female patient taking Depamide (View Usage) (Dosage: ) . Location: FRANCE , 36 years of age, After Depamide was administered, patient had the following side effects: maternal hypertension affecting foetus, oedema peripheral, pre-eclampsia, vaginal infection. During the same period patient was treated with ZOLOFT (Unk) (View Zoloft Review and Zoloft Label ), VALIUM (Unk) (View Valium Review and Valium Label ), STILNOX (View Stilnox Review and Stilnox Label ), TIAPRIDAL (Unk) (View Tiapridal Review and Tiapridal Label ). Patient was hospitalized.

5000981-1 | Coagulation Time Prolonged, International Normalised Ratio Increased
on May 02, 2006 Female patient from FRANCE , 42 years of age, weighting 176.4 lb, was diagnosed with schizophrenia, insomnia, hypothyroidism and was treated with Depamide (View Usage). Patient experienced the following unwanted or unexpected effects: coagulation time prolonged, international normalised ratio increased. Depamide dosage: . During the same period patient was treated with STILNOX (View Stilnox Review and Stilnox Label ), HALDOL (View Haldol Review and Haldol Label ), LEVOTHYROX (View Levothyrox Review and Levothyrox Label ), PREVISCAN (View Previscan Review and Previscan Label ). Patient was hospitalized.


4876020-X | Fall
on Dec 28, 2005 Female patient from FRANCE , 78 years of age, weighting 160.9 lb, was diagnosed with dysthymic disorder, arteritis and was treated with Depamide (View Usage). Patient had the following side effects: fall (What is fall?). Depamide dosage: . During the same period patient was treated with ZOLPIDEM TARTRATE (View Zolpidem Tartrate Review and Zolpidem Tartrate Label ), ANAFRANIL (View Anafranil Review and Anafranil Label ), DEROXAT (View Deroxat Review and Deroxat Label ), ATHYMIL (Unk) (View Athymil Review and Athymil Label ), KARDEGIC (Unk) (View Kardegic Review and Kardegic Label ), CORTANCYL (View Cortancyl Review and Cortancyl Label ), TOPALGIC (Unk) (View Topalgic Review and Topalgic Label ), DIFFU K (Unk) (View Diffu K Review and Diffu K 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 Depamide 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 Depamide quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Depamide 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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Depamide Reactions
Alanine Aminotransferase Increased
Aspartate Aminotransferase Increased
Caesarean Section
CellulitisWhat is Cellulitis?
Coagulation Time Prolonged
Cytolytic Hepatitis
FallWhat is Fall?
Haematology Test Abnormal
International Normalised Ratio Increased
Maternal Hypertension Affecting Foetus
Oedema Peripheral
Pre-eclampsia
Tooth Infection
Vaginal Infection
Depamide 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 Depamide 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!