PROCARDIA Safety Questions, PROCARDIA Answers
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PROCARDIA Safety Reports
Total PROCARDIA reports: 23.PROCARDIA FDA safety alerts: No.
Reported hospitalizations: 7.
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Pharmacist from UNITED STATES reported PROCARDIA problem on Dec 28, 2006. Female patient, weighting 188.9 lb, was diagnosed with hypertension and was treated with PROCARDIA. After drug was administered, patient experienced the following problems/side effects: abdominal pain, arthralgia, back pain, blood pressure inadequately controlled, bronchitis, chest discomfort, chest pain, coronary artery disease, dehydration. PROCARDIA dosage: unknown. During the same period patient was treated with NIFEDIPINE, VASOTEC, COZAAR, HYZAAR, TOPROL, PAXIL. Patient was hospitalized. Patient recovered.
PROCARDIA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 29, 2007. Female patient, weighting 188.9 lb, was diagnosed with hypertension and was treated with PROCARDIA. After drug was administered, patient experienced the following problems/side effects: abdominal pain, arthralgia, back pain, blood pressure inadequately controlled, bronchitis, chest discomfort, chest pain, coronary artery disease, dehydration. PROCARDIA dosage: unknown. During the same period patient was treated with NIFEDIPINE, VASOTEC, COZAAR, HYZAAR, TOPROL, PAXIL. Patient was hospitalized. Patient recovered.
Consumer or non-health professional from UNITED STATES reported PROCARDIA problem on Feb 06, 2007. Female patient, weighting 188.9 lb, was diagnosed with hypertension and was treated with PROCARDIA. After drug was administered, patient experienced the following problems/side effects: abdominal pain, agitation, arthralgia, back pain, blood pressure inadequately controlled, bronchitis, chest discomfort, chest pain, coronary artery disease. PROCARDIA dosage: unknown. During the same period patient was treated with NIFEDIPINE, VASOTEC, COZAAR, HYZAAR, TOPROL, PAXIL. Patient was hospitalized. Patient recovered.
PROCARDIA problem was reported by a Health Professional from UNITED STATES on Feb 10, 2007. Female patient, weighting 130.1 lb, was treated with PROCARDIA. After drug was administered, patient experienced the following problems/side effects: bone pain, oedema peripheral, pain in extremity. PROCARDIA dosage: unknown. During the same period patient was treated with COZAAR. Patient recovered.
Consumer or non-health professional from UNITED STATES reported PROCARDIA problem on Feb 15, 2007. Female patient, weighting 134.9 lb, was diagnosed with hypertension, dyspnoea and was treated with PROCARDIA. After drug was administered, patient experienced the following problems/side effects: bradycardia, dizziness. PROCARDIA dosage: unknown. Patient was hospitalized. Patient recovered.
PROCARDIA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 15, 2007. Female patient, weighting 134.9 lb, was diagnosed with hypertension, dyspnoea and was treated with PROCARDIA. After drug was administered, patient experienced the following problems/side effects: blood pressure inadequately controlled, hysterectomy, mean cell haemoglobin, platelet count decreased. PROCARDIA dosage: unknown. During the same period patient was treated with COZAAR. Patient recovered.
Consumer or non-health professional from UNITED STATES reported PROCARDIA problem on Nov 30, 2006. Female patient, 54 years of age, weighting 220.0 lb, was diagnosed with hypertension and was treated with PROCARDIA. After drug was administered, patient experienced the following problems/side effects: headache, vision blurred. PROCARDIA dosage: 90 MG (90 MG, 1 IN 1 D), ORAL. During the same period patient was treated with HYZAAR, TOPROL, METFORMIN, GLYBURIDE, ACTOS, MAXAIR. Patient recovered.
PROCARDIA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 19, 2007. Female patient, 75 years of age, weighting 130.0 lb, was diagnosed with hypertension, arthritis and was treated with PROCARDIA. After drug was administered, patient experienced the following problems/side effects: abdominal pain lower, anxiety, biopsy endometrium, bowel movement irregularity, breast cancer, breast cyst, breast reconstruction, condition aggravated, constipation. PROCARDIA dosage: unknown. During the same period patient was treated with ENALAPRIL MALEATE, GLUCOSAMINE, VASOTEC, ESTRADERM, PROVERA. Patient recovered.
Health Professional from UNITED STATES reported PROCARDIA problem on Feb 27, 2007. Female patient, weighting 99.21 lb, was diagnosed with hypertension and was treated with PROCARDIA. After drug was administered, patient experienced the following problems/side effects: apnoea, syncope. PROCARDIA dosage: unknown. During the same period patient was treated with CLEVIPREX, LOPRESSOR, PROTONIX, LIPITOR. Patient was hospitalized. Patient recovered.
PROCARDIA problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 24, 2007. Female patient, 82 years of age, was diagnosed with hypertension and was treated with PROCARDIA. After drug was administered, patient experienced the following problems/side effects: atrial fibrillation, autonomic failure syndrome, spinal column stenosis. PROCARDIA dosage: unknown. Patient recovered.
Pharmacist from UNITED STATES reported PROCARDIA problem on Apr 30, 2007. Female patient, weighting 112.0 lb, was diagnosed with raynaud's phenomenon and was treated with PROCARDIA. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased. PROCARDIA dosage: unknown. During the same period patient was treated with REVATIO, PLAVIX. Patient recovered.
PROCARDIA problem was reported by a Physician from UNITED STATES on June 08, 2007. Female patient, weighting 112.0 lb, was diagnosed with raynaud's phenomenon and was treated with PROCARDIA. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased. PROCARDIA dosage: unknown. During the same period patient was treated with REVATIO, PLAVIX, SYNTHROID. Patient recovered.
Consumer or non-health professional from UNITED STATES reported PROCARDIA problem on June 19, 2007. Female patient, weighting 170.0 lb, was diagnosed with hypertension and was treated with PROCARDIA. After drug was administered, patient experienced the following problems/side effects: blood pressure inadequately controlled, dizziness, feeling abnormal. PROCARDIA dosage: unknown. During the same period patient was treated with BENICAR, LANOXIN. Patient recovered.
PROCARDIA problem was reported by a Consumer or non-health professional from UNITED STATES on July 31, 2006. Male patient, 62 years of age, was treated with PROCARDIA. After drug was administered, patient experienced the following problems/side effects: hypersensitivity, pharyngeal oedema, swollen tongue. PROCARDIA dosage: unknown. During the same period patient was treated with MOTRIN, LIPITOR, TOPROL, PLAVIX, ASPIRIN, PROPOXYPHENE AND ACETAMINOPHEN, CLARINEX, ISOSORBIDE MONONITRATE. Patient recovered.
Physician from UNITED STATES reported PROCARDIA problem on Sept 19, 2006. Male patient, 62 years of age, was treated with PROCARDIA. After drug was administered, patient experienced the following problems/side effects: pharyngeal oedema, tongue oedema. PROCARDIA dosage: unknown. During the same period patient was treated with MOTRIN, LIPITOR, TOPROL, PLAVIX, ASPIRIN, PROPOXYPHENE AND ACETAMINOPHEN, CLARINEX, ISOSORBIDE MONONITRATE. Patient recovered.
PROCARDIA problem was reported by a Physician from UNITED STATES on Sept 30, 2006. Male patient, 17 years of age, weighting 200.0 lb, was diagnosed with hypertension and was treated with PROCARDIA. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, aldolase increased, aspartate aminotransferase increased, asthenia, blood creatine phosphokinase increased, fatigue. PROCARDIA dosage: 30 MG (30 MG, DAILY), ORAL. During the same period patient was treated with ATENOLOL. Patient recovered.
Consumer or non-health professional from UNITED STATES reported PROCARDIA problem on Nov 27, 2006. Female patient, 40 years of age, was treated with PROCARDIA. After drug was administered, patient experienced the following problems/side effects: cerebrovascular accident. PROCARDIA dosage: unknown. During the same period patient was treated with ZESTRIL. Patient recovered.
PROCARDIA problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 30, 2006. Female patient, 54 years of age, weighting 220.0 lb, was diagnosed with hypertension and was treated with PROCARDIA. After drug was administered, patient experienced the following problems/side effects: headache, vision blurred. PROCARDIA dosage: 90 MG (90 MG, 1 IN 1 D), ORAL. During the same period patient was treated with HYZAAR, TOPROL, METFORMIN, GLYBURIDE, ACTOS, MAXAIR. Patient recovered.
Consumer or non-health professional from UNITED STATES reported PROCARDIA problem on July 12, 2007. Female patient, weighting 182.4 lb, was diagnosed with hypertension and was treated with PROCARDIA. After drug was administered, patient experienced the following problems/side effects: blood pressure inadequately controlled, cardiac flutter. PROCARDIA dosage: unknown. Patient was hospitalized. Patient recovered.
PROCARDIA problem was reported by a Health Professional from UNITED STATES on July 26, 2007. Male patient, weighting 198.0 lb, was diagnosed with transient ischaemic attack and was treated with PROCARDIA. After drug was administered, patient experienced the following problems/side effects: asthenia, blood sodium decreased, cellulitis, dyspnoea, haemorrhage, paraesthesia, weight increased. PROCARDIA dosage: unknown. During the same period patient was treated with NIFEDIPINE, EXTRA STRENGTH WATER WITH POTASSIUM, LASIX, PLAVIX, ALDACTONE, TAPAZOLE, PROTONIX, ECOTRIN. Patient was hospitalized. Patient recovered.
Consumer or non-health professional from UNITED STATES reported PROCARDIA problem on Aug 09, 2007. Female patient, weighting 104.9 lb, was treated with PROCARDIA. After drug was administered, patient experienced the following problems/side effects: dizziness, loss of consciousness, nausea. PROCARDIA dosage: unknown. During the same period patient was treated with CHLORTHALIDONE. Patient recovered.
PROCARDIA problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 29, 2007. Female patient, weighting 170.0 lb, was diagnosed with hypertension and was treated with PROCARDIA. After drug was administered, patient experienced the following problems/side effects: blood pressure inadequately controlled, dizziness, feeling abnormal. PROCARDIA dosage: unknown. During the same period patient was treated with BENICAR, LANOXIN. Patient recovered.
Consumer or non-health professional from UNITED STATES reported PROCARDIA problem on Sept 07, 2007. Female patient, weighting 104.9 lb, was treated with PROCARDIA. After drug was administered, patient experienced the following problems/side effects: dizziness, loss of consciousness, nausea. PROCARDIA dosage: unknown. During the same period patient was treated with CHLORTHALIDONE. Patient recovered.