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BLOOD CORTICOTROPHIN INCREASED side effect

What is BLOOD CORTICOTROPHIN INCREASED ?
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Drugs associated with BLOOD CORTICOTROPHIN INCREASED

CYCLOSPORINE  DECADRON  METYRAPONE  NEXAVAR  PAXIL  ROZEREM  SANDIMMUNE  SIBUTRAL  


Metyrapone Side Effects Report #5440785-9
Health Professional from JAPAN reported METYRAPONE problem on Aug 21, 2007. Female patient, 66 years of age, weighting 130.5 lb, was diagnosed with pituitary-dependent cushing's syndrome, diabetes mellitus, hypertension and was treated with METYRAPONE. After drug was administered, patient experienced the following problems/side effects: blood corticotrophin increased, cortisol free urine increased, cushingoid, hyperadrenalism, hypertension, pituitary tumour benign, pituitary tumour removal, pituitary-dependent cushing's syndrome, . METYRAPONE dosage: 1250 MG/D. During the same period patient was treated with INSULIN, AMLODIPINE. Patient was hospitalized. Patient recovered.

Nexavar Side Effects Report #5449946-6
NEXAVAR problem was reported by a Physician from UNITED STATES on June 11, 2007. Female patient was treated with NEXAVAR. After drug was administered, patient experienced the following problems/side effects: blood corticotrophin increased, breast tenderness, . NEXAVAR dosage: unknown. Patient recovered.

Rozerem Side Effects Report #5325655-9
Physician from UNITED STATES reported ROZEREM problem on Apr 26, 2007. Female patient was treated with ROZEREM. After drug was administered, patient experienced the following problems/side effects: blood corticotrophin increased, skin discolouration, . ROZEREM dosage: unknown. Patient recovered.

Sibutral Side Effects Report #5419024-0
SIBUTRAL problem was reported by a Health Professional from FRANCE on Aug 08, 2007. Female patient, 27 years of age, weighting 221.1 lb, was diagnosed with obesity, menstrual disorder, gastritis and was treated with SIBUTRAL. After drug was administered, patient experienced the following problems/side effects: angioedema, blood corticotrophin increased, blood pressure decreased, body temperature, cytolytic hepatitis, face oedema, glucose tolerance impaired, loss of consciousness, malaise, . SIBUTRAL dosage: unknown. During the same period patient was treated with BENFLUOREX HYDROCHLORIDE, BENFLUOREX HYDROCHLORIDE, SPASFON, OMEPRAZOLE, ETHINYL ESTRADIOL W, METFORMINE. Patient was hospitalized. Patient recovered.


Cyclosporine Side Effects Report #5348902-6
Consumer or non-health professional from JAPAN reported CYCLOSPORINE problem on May 25, 2007. Male patient, 13 years of age, was diagnosed with nephrotic syndrome and was treated with CYCLOSPORINE. After drug was administered, patient experienced the following problems/side effects: blood antidiuretic hormone increased, blood corticotrophin increased, convulsion, cyclic vomiting syndrome, nephropathy toxic, . CYCLOSPORINE dosage: unknown. Patient was hospitalized. Patient recovered.

Sandimmune Side Effects Report #5356589-1
SANDIMMUNE problem was reported by a Consumer or non-health professional from JAPAN on June 01, 2007. Male patient, 13 years of age, was diagnosed with nephrotic syndrome and was treated with SANDIMMUNE. After drug was administered, patient experienced the following problems/side effects: blood antidiuretic hormone increased, blood corticotrophin increased, convulsion, cyclic vomiting syndrome, nephropathy toxic, . SANDIMMUNE dosage: unknown. During the same period patient was treated with NEORAL. Patient was hospitalized. Patient recovered.

Cyclosporine Side Effects Report #5336798-8
Consumer or non-health professional from JAPAN reported CYCLOSPORINE problem on May 16, 2007. Male patient, 13 years of age, was treated with CYCLOSPORINE. After drug was administered, patient experienced the following problems/side effects: blood antidiuretic hormone increased, blood corticotrophin increased, cyclic vomiting syndrome, nephropathy toxic, . CYCLOSPORINE dosage: unknown. Patient was hospitalized. Patient recovered.

Sibutral Side Effects Report #5286957-8
SIBUTRAL problem was reported by a Health Professional from FRANCE on Mar 28, 2007. Female patient, 27 years of age, weighting 221.1 lb, was diagnosed with menstrual disorder, gastritis and was treated with SIBUTRAL. After drug was administered, patient experienced the following problems/side effects: angioedema, blood corticotrophin increased, blood pressure decreased, body temperature, cytolytic hepatitis, face oedema, glucose tolerance impaired, loss of consciousness, malaise, . SIBUTRAL dosage: unknown. During the same period patient was treated with BENFLUOREX HYDROCHLORIDE, SPASFON, OMEPRAZOLE, ETHINYL ESTRADIOL W. Patient was hospitalized. Patient recovered.

Sibutral Side Effects Report #5297189-1
Health Professional from FRANCE reported SIBUTRAL problem on Apr 05, 2007. Female patient, 27 years of age, weighting 221.1 lb, was diagnosed with obesity, menstrual disorder, gastritis and was treated with SIBUTRAL. After drug was administered, patient experienced the following problems/side effects: angioedema, blood corticotrophin increased, blood pressure decreased, body temperature, cytolytic hepatitis, face oedema, glucose tolerance impaired, loss of consciousness, malaise, . SIBUTRAL dosage: unknown. During the same period patient was treated with BENFLUOREX HYDROCHLORIDE, SPASFON, OMEPRAZOLE, ETHINYL ESTRADIOL W, METFORMIN. Patient was hospitalized. Patient recovered.


Decadron Side Effects Report #5263472-9
DECADRON problem was reported by a Consumer or non-health professional from JAPAN on Feb 28, 2007. Female patient, 31 years of age, was diagnosed with trigeminal neuralgia and was treated with DECADRON. After drug was administered, patient experienced the following problems/side effects: 17-hydroxyprogesterone increased, blood corticotrophin increased, lymphadenopathy, renin decreased, . DECADRON dosage: 0.5 MG/DAY. During the same period patient was treated with CORTRIL, FLORINEF, METLIGINE, TEGRETOL, GLUCOCORTICOIDS. Patient was hospitalized. Patient recovered.

Decadron Side Effects Report #5273317-9
Consumer or non-health professional from JAPAN reported DECADRON problem on Mar 09, 2007. Female patient, 31 years of age, was diagnosed with trigeminal neuralgia and was treated with DECADRON. After drug was administered, patient experienced the following problems/side effects: 17-hydroxyprogesterone increased, blood corticotrophin increased, hyperadrenalism, renin decreased, . DECADRON dosage: 0.5 MG/DAY. During the same period patient was treated with CORTRIL, FLORINEF, METLIGINE, TEGRETOL, GLUCOCORTICOIDS. Patient was hospitalized. Patient recovered.

Sibutral Side Effects Report #5275011-7
SIBUTRAL problem was reported by a Health Professional from FRANCE on Mar 14, 2007. Female patient, 27 years of age, weighting 221.1 lb, was diagnosed with menstrual disorder, gastritis and was treated with SIBUTRAL. After drug was administered, patient experienced the following problems/side effects: angioedema, blood corticotrophin increased, blood pressure decreased, body temperature, cytolytic hepatitis, face oedema, glucose tolerance impaired, loss of consciousness, malaise, . SIBUTRAL dosage: unknown. During the same period patient was treated with BENFLUOREX HYDROCHLORIDE, SPASFON, OMEPRAZOLE, ETHINYL ESTRADIOL W. Patient was hospitalized. Patient recovered.

Rozerem Side Effects Report #5383661-2
Physician from UNITED STATES reported ROZEREM problem on June 26, 2007. Female patient, weighting 105.0 lb, was treated with ROZEREM. After drug was administered, patient experienced the following problems/side effects: adrenal insufficiency, adrenal neoplasm, blood corticotrophin increased, . ROZEREM dosage: unknown. During the same period patient was treated with ANTIHYPERTENSIVE. Patient recovered.

Rozerem Side Effects Report #5383661-2
ROZEREM problem was reported by a Physician from UNITED STATES on June 26, 2007. Female patient, weighting 105.0 lb, was treated with ROZEREM. After drug was administered, patient experienced the following problems/side effects: adrenal insufficiency, adrenal neoplasm, blood corticotrophin increased, . ROZEREM dosage: unknown. During the same period patient was treated with ANTIHYPERTENSIVE. Patient recovered.


Paxil Side Effects Report #5332374-1
Physician from JAPAN reported PAXIL problem on May 17, 2007. Male patient, 55 years of age, weighting 183.0 lb, was diagnosed with depression and was treated with PAXIL. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, blood chloride decreased, blood corticotrophin increased, blood creatinine decreased, blood osmolarity abnormal, blood potassium increased, blood sodium decreased, encephalitis, hyponatraemia, . PAXIL dosage: unknown. During the same period patient was treated with DEPAS, ANTIBIOTICS, ANTIPYRETICS. Patient was hospitalized and became disabled. Patient recovered.

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