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Summary

FDA Adverse Reports: 68. View All

Procardia FDA safety alerts: No

Reported deaths: 5

Reported hospitalizations: 28

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

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Showing 1-50 of 68  Next Page  >

7013462-0 | Dry Skin, Ear Pruritus, Skin Discolouration
on Sep 17, 2010 Female patient from UNITED STATES , weighting 198.0 lb, was diagnosed with hypertension and was treated with Procardia (View Usage). Patient experienced the following unwanted or unexpected effects: dry skin, ear pruritus, skin discolouration. Procardia dosage: 60 Mg, 1x/day.

7006118-1 | Blood Potassium Decreased, Deafness, Depression, Ephelides, Fatigue, Gastric Disorder, Hypotension, Hypovitaminosis, Lethargy
Patient was taking Procardia (View Usage). Patient had the following side effects: blood potassium decreased, deafness, depression (What is depression?), ephelides, fatigue, gastric disorder, hypotension, hypovitaminosis, lethargy on Sep 10, 2010 from UNITED STATES Additional patient health information: Female patient , weighting 95.98 lb, was diagnosed with hypertension, anxiety (What is anxiety?) and. Procardia dosage: 30 Mg, 1x/day. During the same period patient was treated with ATENOLOL (25 Mg, 1x/day) (View Atenolol Review and Atenolol Label ), LORAZEPAM (1 Mg, 4x/day) (View Lorazepam Review and Lorazepam Label ).

6805313-1 | Blood Pressure Decreased, Dizziness, Feeling Abnormal, Hyperhidrosis
Adverse event was reported on Nov 20, 2007 by a Male patient taking Procardia (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: UNITED STATES , weighting 168.0 lb, After Procardia was administered, patient had the following side effects: blood pressure decreased, dizziness (What is dizziness?), feeling abnormal, hyperhidrosis.

6804606-1 | Extrasystoles, Palpitations
on Nov 01, 2007 Female patient from UNITED STATES , weighting 128.0 lb, was diagnosed with hypertension and was treated with Procardia (View Usage). Patient experienced the following unwanted or unexpected effects: extrasystoles, palpitations. Procardia dosage: . During the same period patient was treated with TIAZAC (View Tiazac Review and Tiazac Label ), ULTRAM (View Ultram Review and Ultram Label ), TRAMADOL HCL (View Tramadol Hcl Review and Tramadol Hcl Label ), LORAZEPAM (View Lorazepam Review and Lorazepam Label ).


6804353-6 | Blood Pressure Decreased, Blood Pressure Increased
on Mar 15, 2007 Male patient from UNITED STATES , 87 years of age, was diagnosed with hypertension and was treated with Procardia (View Usage). Patient had the following side effects: blood pressure decreased, blood pressure increased. Procardia dosage: .

6800991-5 | Headache
Patient was taking Procardia (View Usage). After Procardia was administered, patient had the following side effects: headache (What is headache?) on Jan 08, 2008 from UNITED STATES Additional patient health information: Female patient , weighting 155.3 lb, was diagnosed with oesophageal disorder, varices oesophageal and. Procardia dosage: Daily.

6793569-3 | Blood Pressure Increased
Adverse event was reported on Feb 24, 2009 by a Female patient taking Procardia (View Usage) (Dosage: 60 Mg, 1x/day) was diagnosed with hypertension and. Location: UNITED STATES , weighting 165.0 lb, Patient experienced the following unwanted or unexpected effects: blood pressure increased. During the same period patient was treated with ZESTRIL (40 Mg, 1x/day) (View Zestril Review and Zestril Label ), METOPROLOL (Unk) (View Metoprolol Review and Metoprolol Label ).

6792522-3 | Endodontic Procedure, Gingival Recession, Pain In Extremity, Tooth Loss
on Aug 06, 2008 Female patient from UNITED STATES , weighting 120.0 lb, was treated with Procardia (View Usage). Patient had the following side effects: endodontic procedure, gingival recession, pain in extremity, tooth loss. Procardia dosage: .

6788647-9 | Hepatic Steatosis
on Apr 18, 2008 Male patient from UNITED STATES , weighting 167.3 lb, was diagnosed with hypertension and was treated with Procardia (View Usage). After Procardia was administered, patient had the following side effects: hepatic steatosis. Procardia dosage: . During the same period patient was treated with FELODIPINE (View Felodipine Review and Felodipine Label ).

6788255-X | Dizziness, Erythema, Muscle Spasms, Nausea, Palpitations, Pyrexia
Patient was taking Procardia (View Usage). Patient experienced the following unwanted or unexpected effects: dizziness (What is dizziness?), erythema, muscle spasms, nausea (What is nausea?), palpitations, pyrexia on Apr 04, 2008 from UNITED STATES Additional patient health information: Male patient , 74 years of age, . Procardia dosage: .

6554988-3 | Headache, Rash
Adverse event was reported on Jan 26, 2010 by a Female patient taking Procardia (View Usage) (Dosage: One Twice Daily) . Location: UNITED STATES , 57 years of age, weighting 158.0 lb, Patient had the following side effects: headache (What is headache?), rash (What is rash?). Patient was hospitalized.

6539771-7 | Arthralgia, Blood Cholesterol Increased, Blood Pressure Inadequately Controlled, Headache, Nervousness, Ulcer
on Jan 08, 2010 Female patient from UNITED STATES , weighting 209.4 lb, was diagnosed with hypertension, blood cholesterol increased and was treated with Procardia (View Usage). After Procardia was administered, patient had the following side effects: arthralgia, blood cholesterol increased, blood pressure inadequately controlled, headache (What is headache?), nervousness, ulcer (What is ulcer?). Procardia dosage: 30 Mg, 1x/day. During the same period patient was treated with NIFEDIPINE (30 Mg, 1x/day) (View Nifedipine Review and Nifedipine Label ), LIPITOR (Unk) (View Lipitor Review and Lipitor Label ).

6428627-6 | Arthralgia, Blood Cholesterol Increased, Blood Pressure Inadequately Controlled, Headache, Ulcer
on Oct 26, 2009 Female patient from UNITED STATES , weighting 209.4 lb, was diagnosed with hypertension, blood cholesterol increased and was treated with Procardia (View Usage). Patient experienced the following unwanted or unexpected effects: arthralgia, blood cholesterol increased, blood pressure inadequately controlled, headache (What is headache?), ulcer (What is ulcer?). Procardia dosage: 30 Mg, 1x/day. During the same period patient was treated with NIFEDIPINE (30 Mg, 1x/day) (View Nifedipine Review and Nifedipine Label ), LIPITOR (Unk) (View Lipitor Review and Lipitor Label ).

6355274-7 | Hepatic Cirrhosis, Jaundice
Patient was taking Procardia (View Usage). Patient had the following side effects: hepatic cirrhosis, jaundice (What is jaundice?) on Sep 02, 2009 from UNITED STATES Additional patient health information: Female patient , weighting 149.9 lb, was diagnosed with hypertension and. Procardia dosage: 60 Mg, 1x/day. During the same period patient was treated with CYCLOBENZAPRINE (View Cyclobenzaprine Review and Cyclobenzaprine Label ). Patient was hospitalized.

6315375-6 | Hepatic Cirrhosis, Jaundice
Adverse event was reported on Aug 18, 2009 by a Female patient taking Procardia (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: UNITED STATES , weighting 150.0 lb, After Procardia was administered, patient had the following side effects: hepatic cirrhosis, jaundice (What is jaundice?). During the same period patient was treated with CYCLOBENZAPRINE (View Cyclobenzaprine Review and Cyclobenzaprine Label ). Patient was hospitalized.

6267247-3 | Blood Pressure Increased, Pain, Surgery
on Jun 26, 2009 Female patient from UNITED STATES , weighting 112.0 lb, was diagnosed with hypertension and was treated with Procardia (View Usage). Patient experienced the following unwanted or unexpected effects: blood pressure increased, pain (What is pain?), surgery (What is surgery?). Procardia dosage: 60 Mg, 1x/day. During the same period patient was treated with ACCURETIC (View Accuretic Review and Accuretic Label ), LIPITOR (Unk) (View Lipitor Review and Lipitor Label ), VICODIN (Unk) (View Vicodin Review and Vicodin Label ), PLAVIX (Unk) (View Plavix Review and Plavix Label ).

6265473-0 | Hepatic Cirrhosis, Jaundice
on Jul 01, 2009 Female patient from UNITED STATES , weighting 150.0 lb, was diagnosed with hypertension and was treated with Procardia (View Usage). Patient had the following side effects: hepatic cirrhosis, jaundice (What is jaundice?). Procardia dosage: . During the same period patient was treated with CYCLOBENZAPRINE (View Cyclobenzaprine Review and Cyclobenzaprine Label ). Patient was hospitalized.

6261976-3 | Blood Pressure Increased, Pain, Surgery
Patient was taking Procardia (View Usage). After Procardia was administered, patient had the following side effects: blood pressure increased, pain (What is pain?), surgery (What is surgery?) on Jun 30, 2009 from UNITED STATES Additional patient health information: Female patient , weighting 112.0 lb, was diagnosed with hypertension and. Procardia dosage: 60 Mg, 1x/day. During the same period patient was treated with ACCURETIC (View Accuretic Review and Accuretic Label ), LIPITOR (Unk) (View Lipitor Review and Lipitor Label ), VICODIN (Unk) (View Vicodin Review and Vicodin Label ), PLAVIX (Unk) (View Plavix Review and Plavix Label ).

6250567-6 | Blood Pressure Increased, Pain, Surgery
Adverse event was reported on Jun 30, 2009 by a Female patient taking Procardia (View Usage) (Dosage: 60 Mg, 1x/day) was diagnosed with hypertension and. Location: UNITED STATES , weighting 112.0 lb, Patient experienced the following unwanted or unexpected effects: blood pressure increased, pain (What is pain?), surgery (What is surgery?). During the same period patient was treated with ACCURETIC (View Accuretic Review and Accuretic Label ), LIPITOR (Unk) (View Lipitor Review and Lipitor Label ), VICODIN (Unk) (View Vicodin Review and Vicodin Label ), PLAVIX (Unk) (View Plavix Review and Plavix Label ).

6212099-0 | Blood Pressure Increased, Pain, Surgery
on May 14, 2009 Female patient from UNITED STATES , weighting 112.0 lb, was diagnosed with hypertension and was treated with Procardia (View Usage). Patient had the following side effects: blood pressure increased, pain (What is pain?), surgery (What is surgery?). Procardia dosage: 60 Mg, 1x/day. During the same period patient was treated with ACCURETIC (View Accuretic Review and Accuretic Label ), LIPITOR (Unk) (View Lipitor Review and Lipitor Label ), VICODIN (Unk) (View Vicodin Review and Vicodin Label ), PLAVIX (Unk) (View Plavix Review and Plavix Label ).

6196064-8 | Blood Pressure Increased, Pain, Surgery
on May 12, 2009 Female patient from UNITED STATES , weighting 112.0 lb, was diagnosed with hypertension and was treated with Procardia (View Usage). After Procardia was administered, patient had the following side effects: blood pressure increased, pain (What is pain?), surgery (What is surgery?). Procardia dosage: 60 Mg, 1x/day. During the same period patient was treated with ACCURETIC (View Accuretic Review and Accuretic Label ), LIPITOR (Unk) (View Lipitor Review and Lipitor Label ), VICODIN (Unk) (View Vicodin Review and Vicodin Label ), PLAVIX (Unk) (View Plavix Review and Plavix Label ).

6186475-9 | Hypotension
Patient was taking Procardia (View Usage). Patient experienced the following unwanted or unexpected effects: hypotension on May 08, 2009 from UNITED STATES Additional patient health information: Female patient , 84 years of age, . Procardia dosage: .

6072450-1 | Blood Pressure Decreased, Heart Rate Irregular, Teeth Brittle, Tooth Loss
Adverse event was reported on Dec 12, 2008 by a Male patient taking Procardia (View Usage) (Dosage: ) . Location: UNITED STATES , weighting 222.7 lb, Patient had the following side effects: blood pressure decreased, heart rate irregular, teeth brittle, tooth loss. During the same period patient was treated with XANAX (View Xanax Review and Xanax Label ).

6067441-0 | Hypertension, Hypotension, Pancreatic Carcinoma
on Jan 24, 2009 Female patient from UNITED STATES , weighting 103.0 lb, was diagnosed with hypertension, thyroid disorder and was treated with Procardia (View Usage). After Procardia was administered, patient had the following side effects: hypertension, hypotension, pancreatic carcinoma. Procardia dosage: 20 Mg, 1x/day. During the same period patient was treated with LEVOXYL (View Levoxyl Review and Levoxyl Label ), ALBUTEROL (View Albuterol Review and Albuterol Label ), LUNESTA (View Lunesta Review and Lunesta Label ).

6021813-9 | Blood Pressure Decreased, Heart Rate Irregular, Teeth Brittle, Tooth Loss
on Dec 12, 2008 Male patient from UNITED STATES , weighting 222.7 lb, was treated with Procardia (View Usage). Patient experienced the following unwanted or unexpected effects: blood pressure decreased, heart rate irregular, teeth brittle, tooth loss. Procardia dosage: . During the same period patient was treated with XANAX (View Xanax Review and Xanax Label ).

6013793-7 | Hypertension, Hypotension, Pancreatic Carcinoma
Patient was taking Procardia (View Usage). Patient had the following side effects: hypertension, hypotension, pancreatic carcinoma on Dec 08, 2008 from UNITED STATES Additional patient health information: Female patient , weighting 103.0 lb, was diagnosed with hypertension, thyroid disorder and. Procardia dosage: 20 Mg, 1x/day. During the same period patient was treated with LEVOXYL (View Levoxyl Review and Levoxyl Label ), ALBUTEROL (View Albuterol Review and Albuterol Label ), LUNESTA (View Lunesta Review and Lunesta Label ).

5948953-4 | Pulmonary Oedema, Renal Disorder
Adverse event was reported on Oct 31, 2008 by a Female patient taking Procardia (View Usage) (Dosage: ) . Location: UNITED STATES , weighting 118.2 lb, After Procardia was administered, patient had the following side effects: pulmonary oedema, renal disorder. Patient was hospitalized.

5899010-7 | Dialysis, Overdose, Pulmonary Oedema, Renal Failure Chronic
on Sep 15, 2008 Female patient from UNITED STATES , weighting 118.2 lb, was treated with Procardia (View Usage). Patient experienced the following unwanted or unexpected effects: dialysis (What is dialysis?), overdose, pulmonary oedema, renal failure chronic. Procardia dosage: . Patient was hospitalized.

5757628-6 | Anaemia, Blood Glucose Decreased, Cardiac Failure Congestive, Cough, Dehydration, Dyspnoea, Pneumonia, Renal Disorder, Urinary Tract Infection
on May 22, 2008 Female patient from UNITED STATES , weighting 189.4 lb, was diagnosed with hypertension and was treated with Procardia (View Usage). Patient had the following side effects: anaemia, blood glucose decreased, cardiac failure congestive, cough, dehydration, dyspnoea, pneumonia (What is pneumonia?), renal disorder, urinary tract infection (What is urinary tract infection?). Procardia dosage: . During the same period patient was treated with PLENDIL (View Plendil Review and Plendil Label ), COUMADIN (View Coumadin Review and Coumadin Label ). Patient was hospitalized.

5734360-6 | Abdominal Pain Upper, Dyspepsia, Faecaloma, Fear, Haemorrhoidal Haemorrhage, Hernia, Oral Intake Reduced, Weight Decreased
Patient was taking Procardia (View Usage). After Procardia was administered, patient had the following side effects: abdominal pain upper, dyspepsia, faecaloma, fear, haemorrhoidal haemorrhage, hernia (What is hernia?), oral intake reduced, weight decreased on May 08, 2008 from UNITED STATES Additional patient health information: Female patient , 79 years of age, weighting 118.0 lb, was diagnosed with blood pressure (What is blood pressure?) and. Procardia dosage: 60 Mg 1 Daily. During the same period patient was treated with NIFEDIPINE (View Nifedipine Review and Nifedipine Label ). Patient was hospitalized.

5407668-1 | Asthenia, Blood Sodium Decreased, Cellulitis, Dyspnoea, Haemorrhage, Paraesthesia, Weight Increased
Adverse event was reported on Jul 26, 2007 by a Male patient taking Procardia (View Usage) (Dosage: ) was diagnosed with transient ischaemic attack and. Location: UNITED STATES , weighting 198.0 lb, Patient experienced the following unwanted or unexpected effects: asthenia, blood sodium decreased, cellulitis (What is cellulitis?), dyspnoea, haemorrhage, paraesthesia, weight increased. During the same period patient was treated with NIFEDIPINE (View Nifedipine Review and Nifedipine Label ), EXTRA STRENGTH WATER PILL WITH POTASSIUM (View Extra Strength Water Pill With Potassium Review and Extra Strength Water Pill With Potassium Label ), LASIX (View Lasix Review and Lasix Label ), PLAVIX (View Plavix Review and Plavix Label ), ALDACTONE (View Aldactone Review and Aldactone Label ), TAPAZOLE (View Tapazole Review and Tapazole Label ), PROTONIX (View Protonix Review and Protonix Label ), ECOTRIN (View Ecotrin Review and Ecotrin Label ). Patient was hospitalized.

5395949-X | Blood Pressure Inadequately Controlled, Cardiac Flutter
on Jul 12, 2007 Female patient from UNITED STATES , weighting 182.4 lb, was diagnosed with hypertension and was treated with Procardia (View Usage). Patient had the following side effects: blood pressure inadequately controlled, cardiac flutter. Procardia dosage: . Patient was hospitalized.

5362638-7 | Haemoglobin Decreased
on Jun 08, 2007 Female patient from UNITED STATES , weighting 112.0 lb, was diagnosed with raynaud's phenomenon and was treated with Procardia (View Usage). After Procardia was administered, patient had the following side effects: haemoglobin decreased. Procardia dosage: . During the same period patient was treated with REVATIO (View Revatio Review and Revatio Label ), PLAVIX (View Plavix Review and Plavix Label ), SYNTHROID (View Synthroid Review and Synthroid Label ).

5321772-8 | Haemoglobin Decreased
Patient was taking Procardia (View Usage). Patient experienced the following unwanted or unexpected effects: haemoglobin decreased on Apr 30, 2007 from UNITED STATES Additional patient health information: Female patient , weighting 112.0 lb, was diagnosed with raynaud's phenomenon and. Procardia dosage: . During the same period patient was treated with REVATIO (View Revatio Review and Revatio Label ), PLAVIX (View Plavix Review and Plavix Label ).

5317016-3 | Atrial Fibrillation, Autonomic Failure Syndrome, Spinal Column Stenosis
Adverse event was reported on Apr 24, 2007 by a Female patient taking Procardia (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: UNITED STATES , 82 years of age, Patient had the following side effects: atrial fibrillation (What is atrial fibrillation?), autonomic failure syndrome, spinal column stenosis.

5261210-7 | Apnoea, Syncope
on Feb 27, 2007 Female patient from UNITED STATES , weighting 99.21 lb, was diagnosed with hypertension and was treated with Procardia (View Usage). After Procardia was administered, patient had the following side effects: apnoea, syncope. Procardia dosage: . During the same period patient was treated with CLEVIPREX (View Cleviprex Review and Cleviprex Label ), LOPRESSOR (View Lopressor Review and Lopressor Label ), PROTONIX (View Protonix Review and Protonix Label ), LIPITOR (View Lipitor Review and Lipitor Label ). Patient was hospitalized.

5169161-3 | Cerebrovascular Accident
on Nov 27, 2006 Female patient from UNITED STATES , 40 years of age, was treated with Procardia (View Usage). Patient experienced the following unwanted or unexpected effects: cerebrovascular accident. Procardia dosage: . During the same period patient was treated with ZESTRIL (View Zestril Review and Zestril Label ).

5017850-3 | Blood Pressure Increased, Cerebrovascular Accident, Insomnia, Malaise, Memory Impairment, Repetitive Speech, Somnolence
Patient was taking Procardia (View Usage). Patient had the following side effects: blood pressure increased, cerebrovascular accident, insomnia, malaise, memory impairment, repetitive speech, somnolence on May 15, 2006 from UNITED STATES Additional patient health information: Male patient , weighting 280.0 lb, was diagnosed with blood pressure (What is blood pressure?), pain (What is pain?) and. Procardia dosage: . During the same period patient was treated with LYRICA (50 Mg) (View Lyrica Review and Lyrica Label ), OXYCONTIN (View Oxycontin Review and Oxycontin Label ), PLAVIX (View Plavix Review and Plavix Label ), PERCOCET (View Percocet Review and Percocet Label ), ANTIHYPERTENSIVES (View Antihypertensives Review and Antihypertensives Label ), GABAPENTIN (TEVA) (GABAPENTIN) (View Gabapentin (teva) (gabapentin) Review and Gabapentin (teva) (gabapentin) Label ), VITAMIN B12 FOR INJECTION (CYANOCOBALAMIN) (View Vitamin B12 For Injection (cyanocobalamin) Review and Vitamin B12 For Injection (cyanocobalamin) Label ), LUNESTA (View Lunesta Review and Lunesta Label ). Patient was hospitalized.

5001348-2 | Myocardial Infarction
Adverse event was reported on May 02, 2006 by a Female patient taking Procardia (View Usage) (Dosage: ) was diagnosed with arthritis (What is arthritis?) and. Location: UNITED STATES , 59 years of age, weighting 160.9 lb, After Procardia was administered, patient had the following side effects: myocardial infarction. During the same period patient was treated with ZESTRIL (View Zestril Review and Zestril Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), PRILOSEC (View Prilosec Review and Prilosec Label ), CYCLOBENZAPRINE HYDROCHLORIDE (View Cyclobenzaprine Hydrochloride Review and Cyclobenzaprine Hydrochloride Label ), VIOXX (View Vioxx Review and Vioxx Label ). Patient was hospitalized.

4995965-3 | Abdominal Pain Upper, Angina Pectoris, Arteriospasm Coronary, Arthropathy, Back Injury, Blood Pressure Increased, Chest Pain, Dyspnoea Exertional
on Nov 03, 2005 Female patient from UNITED STATES , 42 years of age, weighting 224.9 lb, was diagnosed with arthralgia, arthritis (What is arthritis?) and was treated with Procardia (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain upper, angina pectoris, arteriospasm coronary, arthropathy, back injury, blood pressure increased, chest pain (What is chest pain?), dyspnoea exertional. Procardia dosage: . During the same period patient was treated with ZELNORM (View Zelnorm Review and Zelnorm Label ), VIOXX (View Vioxx Review and Vioxx Label ), PREVPAC (View Prevpac Review and Prevpac Label ), PROTONIX (View Protonix Review and Protonix Label ), ANASPAZ (View Anaspaz Review and Anaspaz Label ), ERYTHROMYCIN (View Erythromycin Review and Erythromycin Label ). Patient was hospitalized and became disabled.

4968839-1 | Blood Pressure Increased, Renal Failure, Renal Transplant
on Mar 25, 2006 Male patient from UNITED STATES , 66 years of age, weighting 300.0 lb, was diagnosed with hypertension and was treated with Procardia (View Usage). Patient had the following side effects: blood pressure increased, renal failure, renal transplant. Procardia dosage: . During the same period patient was treated with PROCARDIA XL (View Procardia Xl Review and Procardia Xl Label ).

4919135-X | Blood Pressure Increased, Renal Failure, Renal Transplant
Patient was taking Procardia (View Usage). After Procardia was administered, patient had the following side effects: blood pressure increased, renal failure, renal transplant on Feb 06, 2006 from UNITED STATES Additional patient health information: Male patient , 66 years of age, weighting 300.0 lb, was diagnosed with hypertension and. Procardia dosage: . During the same period patient was treated with PROCARDIA XL (View Procardia Xl Review and Procardia Xl Label ).

4909852-X | Anxiety, Depression, Hypothyroidism, Impaired Work Ability, Mental Disorder, Nervousness
Adverse event was reported on Jan 30, 2006 by a Female patient taking Procardia (View Usage) (Dosage: 20 Or 30 Milligram (daily), Oral) was diagnosed with vasodilatation, depression (What is depression?), nervousness and. Location: UNITED STATES , 45 years of age, Patient experienced the following unwanted or unexpected effects: anxiety (What is anxiety?), depression (What is depression?), hypothyroidism, impaired work ability, mental disorder, nervousness. During the same period patient was treated with ZOLOFT (100 Mg (100 Mg, Daily), Oral) (View Zoloft Review and Zoloft Label ), LEVOXYL (View Levoxyl Review and Levoxyl Label ), INSULIN (View Insulin Review and Insulin Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), XANAX (0.5 Mg (0.5 Mg, Prn), Oral) (View Xanax Review and Xanax Label ). Patient was hospitalized and became disabled.

4896151-8 | Depression, Hypothyroidism, Mental Disorder, Nervousness
on Jan 16, 2006 Female patient from UNITED STATES , 45 years of age, was diagnosed with vasodilatation, depression (What is depression?), nervousness and was treated with Procardia (View Usage). Patient had the following side effects: depression (What is depression?), hypothyroidism, mental disorder, nervousness. Procardia dosage: 20 Or 30 Milligram (daily), Oral. During the same period patient was treated with ZOLOFT (100 Mg (100 Mg, Daily), Oral) (View Zoloft Review and Zoloft Label ), XANAX (0.5 Mg (0.5 Mg, Prn), Oral) (View Xanax Review and Xanax Label ), LEVOXYL (View Levoxyl Review and Levoxyl Label ), INSULIN (View Insulin Review and Insulin Label ), ASPIRIN (View Aspirin Review and Aspirin Label ). Patient was hospitalized and became disabled.

4880660-1 | Joint Injury, Pulmonary Embolism
on Jun 07, 2005 Female patient from UNITED STATES , 68 years of age, weighting 231.5 lb, was diagnosed with arthralgia and was treated with Procardia (View Usage). After Procardia was administered, patient had the following side effects: joint injury, pulmonary embolism (What is pulmonary embolism?). Procardia dosage: . During the same period patient was treated with DIOVAN (View Diovan Review and Diovan Label ), HYDRODIURIL (View Hydrodiuril Review and Hydrodiuril Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), VIOXX (View Vioxx Review and Vioxx Label ). Patient was hospitalized and became disabled.

4871306-7 | Dialysis, Renal Failure, Renal Transplant
Patient was taking Procardia (View Usage). Patient experienced the following unwanted or unexpected effects: dialysis (What is dialysis?), renal failure, renal transplant on Dec 19, 2005 from UNITED STATES Additional patient health information: Male patient , weighting 200.0 lb, was diagnosed with hypertension and. Procardia dosage: 90 Mg (90 Mg, Daily Interval: Every Day). During the same period patient was treated with PROGRAF (View Prograf Review and Prograf Label ), BACTRIM (View Bactrim Review and Bactrim Label ), LOPRESSOR (View Lopressor Review and Lopressor Label ), VALCYTE (View Valcyte Review and Valcyte Label ), HUMULIN R (View Humulin R Review and Humulin R Label ), HUMULIN N (View Humulin N Review and Humulin N Label ), PREDNISONE (View Prednisone Review and Prednisone Label ).

4838393-3 | Depression, Fibromyalgia, Gastric Bypass, Nerve Injury, Osteoarthritis
Adverse event was reported on Nov 14, 2005 by a Female patient taking Procardia (View Usage) (Dosage: 90 Mg (90 Mg, Daily Interval: Every Day), Oral) was diagnosed with hypertension and. Location: UNITED STATES , 43 years of age, weighting 125.0 lb, Patient had the following side effects: depression (What is depression?), fibromyalgia, gastric bypass, nerve injury, osteoarthritis (What is osteoarthritis?). During the same period patient was treated with FENTANYL (View Fentanyl Review and Fentanyl Label ), PLAVIX (View Plavix Review and Plavix Label ), VERAPAMIL (View Verapamil Review and Verapamil Label ), FOSAMAX (View Fosamax Review and Fosamax Label ), PAMELOR (View Pamelor Review and Pamelor Label ), LASIX (View Lasix Review and Lasix Label ).

4830199-4 | Adverse Event, Cardiac Disorder, Cataract, Dermatitis, Glaucoma, Oesophageal Varices Haemorrhage, Osteoarthritis, Rheumatoid Arthritis, Upper Gastrointestinal Haemorrhage
on Mar 12, 2004 Female patient from UNITED STATES , 79 years of age, weighting 105.8 lb, was diagnosed with hypertension, rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Procardia (View Usage). After Procardia was administered, patient had the following side effects: adverse event, cardiac disorder, cataract (What is cataract?), dermatitis, glaucoma (What is glaucoma?), oesophageal varices haemorrhage, osteoarthritis (What is osteoarthritis?), rheumatoid arthritis (What is rheumatoid arthritis?), upper gastrointestinal haemorrhage. Procardia dosage: . During the same period patient was treated with VIOXX (View Vioxx Review and Vioxx Label ), LOTENSIN (View Lotensin Review and Lotensin Label ), VASOTEC (View Vasotec Review and Vasotec Label ), TENORMIN (View Tenormin Review and Tenormin Label ), TOPROL XL (View Toprol-xl Review and Toprol-xl Label ), CARDIZEM (View Cardizem Review and Cardizem Label ), HYTRIN (View Hytrin Review and Hytrin Label ).

4824252-9 | Dialysis, Renal Failure, Renal Transplant
on Oct 26, 2005 Male patient from UNITED STATES , weighting 200.0 lb, was diagnosed with hypertension and was treated with Procardia (View Usage). Patient experienced the following unwanted or unexpected effects: dialysis (What is dialysis?), renal failure, renal transplant. Procardia dosage: 90 Mg (90 Mg, Daily Interval: Every Day). During the same period patient was treated with PROGRAF (View Prograf Review and Prograf Label ), BACTRIM (View Bactrim Review and Bactrim Label ), LOPRESSOR (View Lopressor Review and Lopressor Label ), VALCYTE (View Valcyte Review and Valcyte Label ), HUMULIN R (View Humulin R Review and Humulin R Label ), HUMULIN N (View Humulin N Review and Humulin N Label ), PREDNISONE (View Prednisone Review and Prednisone Label ).

4818809-9 | Arthritis, Blood Cholesterol Increased, Cholelithiasis, Economic Problem, Hepatic Function Abnormal, Impaired Work Ability, Malaise, Mobility Decreased
Patient was taking Procardia (View Usage). Patient had the following side effects: arthritis (What is arthritis?), blood cholesterol increased, cholelithiasis, economic problem, hepatic function abnormal, impaired work ability, malaise, mobility decreased on Oct 21, 2005 from UNITED STATES Additional patient health information: Female patient , weighting 300.0 lb, was diagnosed with hypertension, blood cholesterol increased, ill-defined disorder, arthritis (What is arthritis?) and. Procardia dosage: . During the same period patient was treated with LIPITOR (View Lipitor Review and Lipitor Label ), ZOLOFT (View Zoloft Review and Zoloft Label ).

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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 Procardia 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 Procardia quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Procardia 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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Post Procardia Side Effect Reporting Your Procardia side effect will help others recognize and deal with Procardia side effects. Recent Reports View Procardia reports ...

I've been trying to figure this out the last 45 min! a. digoxin (Lanoxin) b. nitroglycerin (NitroBid) c. nifedipine (Procardia) d. doxazosin (Cardura)

During the same period patient was treated with PROCARDIA XL (Qd: Every Day) (View Procardia Xl Review and Procardia Xl Label ), LIPITOR (Daily: Every Day) (View Lipitor ...

About Lopressor : Risks and Benefits, News and Updates, Lopressor video and TV resources

High blood pressure , also called hypertension, usually

NASAL CONGESTION, view Drugs and Side Effects associated with NASAL CONGESTION, ,NASAL CONGESTION ENBREL,NASAL CONGESTION HUMIRA,NASAL CONGESTION ULTRAVIST,NASAL ...

So my MD switched me to Procardia XL (calcium channel blocker). I had even more reaction to the Procardia XL and ended up in the hospital. Yesterday my Cardiologist, not ...

Micardis Side Effects - Complete Patient's Guide | User Reviews: Male patient, 32 years of age, weighting 125.7 |Imsomnia|Fatigue|Imsomnia And Head Ache And Fatigue ...

During the same period patient was treated with NEORAL (View Neoral Review and Neoral Label ), PROCARDIA XL (NIFEDINE) (NIFEDIPINE) (View Procardia Xl (nifedine) (nifedipine ...

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Procardia Reactions
Abdominal Distension
Blood Cholesterol Increased
Blood Creatinine Increased
Blood Pressure Decreased
Blood Pressure Inadequately Controlled
Blood Pressure Increased
Blood Urea Increased
Carotid Artery Stenosis
Cerebrovascular Accident
Compression Fracture
DepressionWhat is Depression?
DialysisWhat is Dialysis?
Femoral Artery Occlusion
Gastrointestinal Haemorrhage
Haemoglobin Decreased
HeadacheWhat is Headache?
Hepatic Cirrhosis
Hot Flush
Hypertension
Hypotension
JaundiceWhat is Jaundice?
Menorrhagia
Nervousness
PainWhat is Pain?
RashWhat is Rash?
Renal Failure
Renal Transplant
Speech Disorder
SurgeryWhat is Surgery?
Tooth Loss
Procardia 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 Procardia 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!