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Aldactazide adverse events reported to FDA.

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Summary

FDA Adverse Reports: 11. View All

Aldactazide FDA safety alerts: No

Reported deaths: 2

Reported hospitalizations: 4

Aldactazide Dosage, Warnings, Usage.

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

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6793803-X | Blood Pressure Increased, Fluid Retention, Weight Increased
on May 08, 2009 Female patient from UNITED STATES , weighting 130.1 lb, was diagnosed with hypothyroidism and was treated with Aldactazide (View Usage). Patient experienced the following unwanted or unexpected effects: blood pressure increased, fluid retention, weight increased. Aldactazide dosage: 50 Mg, 2x/day. During the same period patient was treated with SYNTHROID (Unk) (View Synthroid Review and Synthroid Label ).

6788449-3 | Hyperthyroidism, Hypothyroidism
Patient was taking Aldactazide (View Usage). Patient had the following side effects: hyperthyroidism, hypothyroidism on Mar 04, 2008 from UNITED STATES Additional patient health information: Female patient , weighting 160.0 lb, was diagnosed with fluid retention, hypothyroidism and. Aldactazide dosage: 25/25 Mg. During the same period patient was treated with LASIX (View Lasix Review and Lasix Label ).

5304964-3 | Face Oedema, Hypoaesthesia, Lip Swelling
Adverse event was reported on Apr 12, 2007 by a Female patient taking Aldactazide (View Usage) (Dosage: Daily Dose:25mg) was diagnosed with oedema and. Location: JAPAN , 58 years of age, After Aldactazide was administered, patient had the following side effects: face oedema, hypoaesthesia, lip swelling. During the same period patient was treated with ZYLORIC ^FRESENIUS^ (View Zyloric ^fresenius^ Review and Zyloric ^fresenius^ Label ), CALTAN (View Caltan Review and Caltan Label ), LIPITOR (View Lipitor Review and Lipitor Label ), LENDORMIN (View Lendormin Review and Lendormin Label ), MYSLEE (View Myslee Review and Myslee Label ), ZANTAC (View Zantac Review and Zantac Label ), BLOPRESS (View Blopress Review and Blopress Label ), LUVOX (View Luvox Review and Luvox Label ).

5296886-1 | Face Oedema, Hypoaesthesia, Lip Swelling
on Apr 05, 2007 Female patient from JAPAN , 58 years of age, was treated with Aldactazide (View Usage). Patient experienced the following unwanted or unexpected effects: face oedema, hypoaesthesia, lip swelling. Aldactazide dosage: Daily Dose:25mg. During the same period patient was treated with ZYLORIC ^FRESENIUS^ (View Zyloric ^fresenius^ Review and Zyloric ^fresenius^ Label ), CALTAN (View Caltan Review and Caltan Label ), LIPITOR (View Lipitor Review and Lipitor Label ), LENDORMIN (View Lendormin Review and Lendormin Label ), MYSLEE (View Myslee Review and Myslee Label ), ZANTAC (View Zantac Review and Zantac Label ), BLOPRESS (View Blopress Review and Blopress Label ), LUVOX (View Luvox Review and Luvox Label ).


5285312-4 | Asthenia, Malaise, Muscle Spasms, Renal Failure Acute
on Mar 26, 2007 Female patient from SPAIN , 85 years of age, was diagnosed with cardiac failure, ischaemic cardiomyopathy and was treated with Aldactazide (View Usage). Patient had the following side effects: asthenia, malaise, muscle spasms, renal failure acute. Aldactazide dosage: . During the same period patient was treated with SEGURIL (View Seguril Review and Seguril Label ), ACOVIL (View Acovil Review and Acovil Label ), CORDIPLAST (Daily Dose:10mg) (View Cordiplast Review and Cordiplast Label ), TROMALYT (Daily Dose:150mg) (View Tromalyt Review and Tromalyt Label ), LOSEC (Daily Dose:20mg) (View Losec Review and Losec Label ). Patient was hospitalized.

5192428-X | Blood Glucose Decreased, Blood Pressure Increased, Diabetes Mellitus, Face Oedema, Feeling Abnormal, Head Injury, Hypotension, Infection, Localised Oedema
Patient was taking Aldactazide (View Usage). After Aldactazide was administered, patient had the following side effects: blood glucose decreased, blood pressure increased, diabetes mellitus, face oedema, feeling abnormal, head injury, hypotension, infection (What is infection?), localised oedema on Dec 09, 2006 from UNITED STATES Additional patient health information: Female patient , 63 years of age, weighting 185.0 lb, was diagnosed with hypertension and. Aldactazide dosage: . During the same period patient was treated with TAURINE (View Taurine Review and Taurine Label ), PENICILLINE (BENZYLPENICILLIN SODIUM) (View Penicilline (benzylpenicillin Sodium) Review and Penicilline (benzylpenicillin Sodium) Label ).

5155425-6 | Blood Glucose Decreased, Blood Pressure Increased, Diabetes Mellitus, Feeling Abnormal, Fluid Retention, Head Injury, Hypotension, Ill-defined Disorder, Infection
Adverse event was reported on Nov 01, 2006 by a Female patient taking Aldactazide (View Usage) (Dosage: ) . Location: UNITED STATES , 63 years of age, weighting 185.0 lb, Patient experienced the following unwanted or unexpected effects: blood glucose decreased, blood pressure increased, diabetes mellitus, feeling abnormal, fluid retention, head injury, hypotension, ill-defined disorder, infection (What is infection?). During the same period patient was treated with TAURINE (TAURINE) (View Taurine (taurine) Review and Taurine (taurine) Label ), PENICILLINE (BENZYLPENICILLIN SODIUM) (View Penicilline (benzylpenicillin Sodium) Review and Penicilline (benzylpenicillin Sodium) Label ).

5142567-4 | Blood Pressure Increased, Heart Rate Irregular, Palpitations, Sensory Disturbance, Tachycardia
on Oct 16, 2006 Female patient from UNITED STATES , 63 years of age, was treated with Aldactazide (View Usage). Patient had the following side effects: blood pressure increased, heart rate irregular, palpitations, sensory disturbance, tachycardia. Aldactazide dosage: .

4957740-5 | Blister, Hypokalaemia, Hyponatraemia, Hypotension, Oedema Peripheral
on Mar 13, 2006 Female patient from UNITED STATES , 67 years of age, was diagnosed with ill-defined disorder and was treated with Aldactazide (View Usage). After Aldactazide was administered, patient had the following side effects: blister, hypokalaemia, hyponatraemia, hypotension, oedema peripheral. Aldactazide dosage: . During the same period patient was treated with LASIX (View Lasix Review and Lasix Label ), GLUCOVANCE (View Glucovance Review and Glucovance Label ), ALPRAZOLAM (View Alprazolam Review and Alprazolam Label ), POTASSIUM CHLORIDE (View Potassium Chloride Review and Potassium Chloride Label ), ZOLOFT (View Zoloft Review and Zoloft Label ), PREVACID (LANSPORAZOLE) (View Prevacid (lansporazole) Review and Prevacid (lansporazole) Label ). Patient was hospitalized.

4674034-6 | Adenocarcinoma Pancreas, Confusional State, Haemoglobin Increased, Hypochloraemia, Hypoglycaemia, Hyponatraemia, Pain
Patient was taking Aldactazide (View Usage). Patient experienced the following unwanted or unexpected effects: adenocarcinoma pancreas, confusional state, haemoglobin increased, hypochloraemia, hypoglycaemia, hyponatraemia, pain (What is pain?) on May 13, 2005 from Additional patient health information: Female patient , 70 years of age, weighting 165.3 lb, was diagnosed with hypertension and. Aldactazide dosage: 1 Df (od), Oral. During the same period patient was treated with LITHIUM CARBOANTE (LITHIUM CARBONATE) (View Lithium Carboante (lithium Carbonate) Review and Lithium Carboante (lithium Carbonate) Label ), METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ), GLIQUIDONE (GLIQUIDONE) (View Gliquidone (gliquidone) Review and Gliquidone (gliquidone) Label ), INSULIN (View Insulin Review and Insulin Label ), PARACETAMOL (PARACETAMOL) (View Paracetamol (paracetamol) Review and Paracetamol (paracetamol) Label ), NSAID'S (NSAID'S) (View Nsaid's (nsaid's) Review and Nsaid's (nsaid's) Label ). Patient was hospitalized.

4596420-5 | Adenocarcinoma Pancreas, Back Pain, Blood Pressure Increased, Confusional State, Haemoglobin Increased, Hypochloraemia, Hypoglycaemia, Hyponatraemia, Malignant Neoplasm Progression
Adverse event was reported on Feb 15, 2005 by a Female patient taking Aldactazide (View Usage) (Dosage: 1 Df (od), Oral) was diagnosed with hypertension and. Location: , 70 years of age, weighting 165.3 lb, Patient had the following side effects: adenocarcinoma pancreas, back pain (What is back pain?), blood pressure increased, confusional state, haemoglobin increased, hypochloraemia, hypoglycaemia, hyponatraemia, malignant neoplasm progression. During the same period patient was treated with LITHIUM CARBONATE (View Lithium Carbonate Review and Lithium Carbonate Label ), METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ), GLIQUIDONE (GLIQUIDONE) (View Gliquidone (gliquidone) Review and Gliquidone (gliquidone) Label ), INSULIN (View Insulin Review and Insulin Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), NSAID'S (NSAID'S) (View Nsaid's (nsaid's) Review and Nsaid's (nsaid's) 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 Aldactazide 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 Aldactazide quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Aldactazide 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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Aldactazide Reactions
Adenocarcinoma Pancreas
Asthenia
Back PainWhat is Back pain?
Blister
Blood Glucose Decreased
Blood Pressure Increased
Confusional State
Diabetes Mellitus
Face Oedema
Feeling Abnormal
Fluid Retention
Haemoglobin Increased
Head Injury
Heart Rate Irregular
Hyperthyroidism
Hypoaesthesia
Hypochloraemia
Hypoglycaemia
Hypokalaemia
Hyponatraemia
Hypotension
Hypothyroidism
Ill-defined Disorder
InfectionWhat is Infection?
Lip Swelling
Localised Oedema
Malaise
Malignant Neoplasm Progression
Muscle Spasms
Oedema Peripheral
Aldactazide 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 Aldactazide 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!