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Perdipine adverse events reported to FDA.

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Summary

FDA Adverse Reports: 25. View All

Perdipine FDA safety alerts: No

Reported deaths: 4

Reported hospitalizations: 17

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

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6702306-X | Papuloerythroderma Of Ofuji
on Apr 27, 2010 Male patient from JAPAN , 60 years of age, was diagnosed with renal hypertension and was treated with Perdipine (View Usage). Patient experienced the following unwanted or unexpected effects: papuloerythroderma of ofuji. Perdipine dosage: . During the same period patient was treated with EMABERIN (View Emaberin Review and Emaberin Label ), FLUITRAN (View Fluitran Review and Fluitran Label ).

6626026-5 | Papuloerythroderma Of Ofuji
Patient was taking Perdipine (View Usage). Patient had the following side effects: papuloerythroderma of ofuji on Mar 03, 2010 from JAPAN Additional patient health information: Male patient , 60 years of age, was diagnosed with renal hypertension and. Perdipine dosage: . During the same period patient was treated with EMABERIN (View Emaberin Review and Emaberin Label ), FLUITRAN (View Fluitran Review and Fluitran Label ).

5743115-8 | Cerebral Haemorrhage
Adverse event was reported on Mar 27, 2008 by a Male patient taking Perdipine (View Usage) (Dosage: Unk) was diagnosed with hypertension, stomatitis, diarrhoea, abdominal pain upper, nausea (What is nausea?), constipation (What is constipation?), headache (What is headache?), prophylaxis and. Location: JAPAN , weighting 119.0 lb, After Perdipine was administered, patient had the following side effects: cerebral haemorrhage. During the same period patient was treated with DEXALTIN (Unk) (View Dexaltin Review and Dexaltin Label ), LOPEMIN (Unk) (View Lopemin Review and Lopemin Label ), OMEPRAZOLE (20 Mg) (View Omeprazole Review and Omeprazole Label ), SM (1 Df) (View Sm Review and Sm Label ), MAGLAX (Unk) (View Maglax Review and Maglax Label ), GLYSENNID (Unk) (View Glysennid Review and Glysennid Label ), LOXONIN (Unk) (View Loxonin Review and Loxonin Label ), MUCOSTA (Unk) (View Mucosta Review and Mucosta Label ). Patient was hospitalized.

5701593-4 | Cerebral Haemorrhage
on Mar 27, 2008 Male patient from JAPAN , weighting 119.0 lb, was diagnosed with hypertension, stomatitis, diarrhoea, abdominal pain upper, nausea (What is nausea?), constipation (What is constipation?), headache (What is headache?), prophylaxis and was treated with Perdipine (View Usage). Patient experienced the following unwanted or unexpected effects: cerebral haemorrhage. Perdipine dosage: Unk. During the same period patient was treated with DEXALTIN (Unk) (View Dexaltin Review and Dexaltin Label ), LOPEMIN (Unk) (View Lopemin Review and Lopemin Label ), OMEPRAL (20 Mg) (View Omepral Review and Omepral Label ), SM (1 Df) (View Sm Review and Sm Label ), MAGLAX (Unk) (View Maglax Review and Maglax Label ), GLYSENNID (Unk) (View Glysennid Review and Glysennid Label ), LOXONIN (Unk) (View Loxonin Review and Loxonin Label ), MUCOSTA (Unk) (View Mucosta Review and Mucosta Label ). Patient was hospitalized.


5701592-2 | Cerebral Haemorrhage
on Mar 27, 2008 Male patient from JAPAN , weighting 119.0 lb, was diagnosed with hypertension, stomatitis, diarrhoea, abdominal pain upper, nausea (What is nausea?), constipation (What is constipation?), headache (What is headache?), prophylaxis and was treated with Perdipine (View Usage). Patient had the following side effects: cerebral haemorrhage. Perdipine dosage: Unk. During the same period patient was treated with DEXALTIN (Unk) (View Dexaltin Review and Dexaltin Label ), LOPEMIN (Unk) (View Lopemin Review and Lopemin Label ), OMEPRAL (20 Mg) (View Omepral Review and Omepral Label ), SM (1 Df) (View Sm Review and Sm Label ), MAGLAX (Unk) (View Maglax Review and Maglax Label ), GLYSENNID (Unk) (View Glysennid Review and Glysennid Label ), LOXONIN (Unk) (View Loxonin Review and Loxonin Label ), MUCOSTA (Unk) (View Mucosta Review and Mucosta Label ). Patient was hospitalized.

5642823-7 | Cerebral Haemorrhage
Patient was taking Perdipine (View Usage). After Perdipine was administered, patient had the following side effects: cerebral haemorrhage on Feb 18, 2008 from JAPAN Additional patient health information: Male patient , weighting 119.0 lb, was diagnosed with hypertension, stomatitis, diarrhoea, abdominal pain upper, nausea (What is nausea?), constipation (What is constipation?), headache (What is headache?), prophylaxis and. Perdipine dosage: . During the same period patient was treated with DEXALTIN (View Dexaltin Review and Dexaltin Label ), LOPEMIN (View Lopemin Review and Lopemin Label ), OMEPRAL (20 Mg) (View Omepral Review and Omepral Label ), SM (1.3 G) (View Sm Review and Sm Label ), MAGLAX (View Maglax Review and Maglax Label ), GLYSENNID (View Glysennid Review and Glysennid Label ), LOXONIN (View Loxonin Review and Loxonin Label ), MUCOSTA (View Mucosta Review and Mucosta Label ). Patient was hospitalized.

5406928-8 | Stevens-johnson Syndrome
Adverse event was reported on Jul 23, 2007 by a Male patient taking Perdipine (View Usage) (Dosage: Daily Dose Reported: Increased Or Decreased Based On Blood Pressure, On An As Needed Basis.) was diagnosed with hypertension, pyrexia, convulsion prophylaxis and. Location: JAPAN , 70 years of age, Patient experienced the following unwanted or unexpected effects: stevens-johnson syndrome. During the same period patient was treated with NAPROXEN (View Naproxen Review and Naproxen Label ), ROHYPNOL (View Rohypnol Review and Rohypnol Label ), CERCINE (View Cercine Review and Cercine Label ), MYSLEE (View Myslee Review and Myslee Label ).

5406187-6 | Stevens-johnson Syndrome
on Jul 23, 2007 Male patient from JAPAN , 70 years of age, was diagnosed with hypertension, pyrexia, convulsion prophylaxis and was treated with Perdipine (View Usage). Patient had the following side effects: stevens-johnson syndrome. Perdipine dosage: Daily Dose Reported: Increased Or Decreased Based On Blood Pressure, On An As Needed Basis.. During the same period patient was treated with NAPROXEN (View Naproxen Review and Naproxen Label ), ROHYPNOL (View Rohypnol Review and Rohypnol Label ), CERCINE (View Cercine Review and Cercine Label ), MYSLEE (View Myslee Review and Myslee Label ).

5401512-4 | Stevens-johnson Syndrome
on Jul 23, 2007 Male patient from JAPAN , 70 years of age, was diagnosed with hypertension, pyrexia, convulsion prophylaxis and was treated with Perdipine (View Usage). After Perdipine was administered, patient had the following side effects: stevens-johnson syndrome. Perdipine dosage: Daily Dose Reported: Increased Or Decreased Based On Blood Pressure, On An As Needed Basis.. During the same period patient was treated with NAPROXEN (View Naproxen Review and Naproxen Label ), ROHYPNOL (View Rohypnol Review and Rohypnol Label ), CERCINE (View Cercine Review and Cercine Label ), MYSLEE (View Myslee Review and Myslee Label ).

5392301-8 | Stevens-johnson Syndrome
Patient was taking Perdipine (View Usage). Patient experienced the following unwanted or unexpected effects: stevens-johnson syndrome on Jul 09, 2007 from JAPAN Additional patient health information: Male patient , 70 years of age, was diagnosed with hypertension, pyrexia, convulsion prophylaxis and. Perdipine dosage: Daily Dose Reported: Increased Or Decreased Based On Blood Pressure, On An As Needed Basis.. During the same period patient was treated with NAPROXEN (View Naproxen Review and Naproxen Label ), ROHYPNOL (View Rohypnol Review and Rohypnol Label ), CERCINE (View Cercine Review and Cercine Label ), MYSLEE (View Myslee Review and Myslee Label ).

5365588-5 | Abdominal Pain, Disseminated Intravascular Coagulation, Inflammatory Bowel Disease
Adverse event was reported on Jun 13, 2007 by a Male patient taking Perdipine (View Usage) (Dosage: Dose Reported As 96 Mg Continuous; 4 Ml/hour) was diagnosed with hypertension and. Location: JAPAN , 29 years of age, weighting 224.9 lb, Patient had the following side effects: abdominal pain (What is abdominal pain?), disseminated intravascular coagulation, inflammatory bowel disease. During the same period patient was treated with NORVASC (View Norvasc Review and Norvasc Label ), NU LOTAN (View Nu-lotan Review and Nu-lotan Label ).

5338781-5 | Ileus Paralytic
on Jul 27, 2006 Male patient from JAPAN , 68 years of age, weighting 103.4 lb, was diagnosed with blood pressure management and was treated with Perdipine (View Usage). After Perdipine was administered, patient had the following side effects: ileus paralytic. Perdipine dosage: Duration:14 Hrs 55 Min: 24 July 2006, 1.35 P.m. 2.0 Ml/hr, 2:00 P.m. Increased To 3.0 Ml/hr, 5:00 P+. During the same period patient was treated with ATROPINE SULFATE (View Atropine Sulfate Review and Atropine Sulfate Label ), CLARITHROMYCIN (View Clarithromycin Review and Clarithromycin Label ). Patient was hospitalized.

5332291-7 | Abdominal Pain, Bacteraemia, Disseminated Intravascular Coagulation, Haemodialysis, Inflammatory Bowel Disease
on May 15, 2007 Male patient from JAPAN , 29 years of age, weighting 224.9 lb, was diagnosed with hypertension and was treated with Perdipine (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain (What is abdominal pain?), bacteraemia, disseminated intravascular coagulation, haemodialysis, inflammatory bowel disease. Perdipine dosage: 120 Ml Daily. During the same period patient was treated with NORVASC (View Norvasc Review and Norvasc Label ), NU LOTAN (View Nu-lotan Review and Nu-lotan Label ).

5288267-1 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Erythema Multiforme, Hepatic Function Abnormal, Purpura
Patient was taking Perdipine (View Usage). Patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood lactate dehydrogenase increased, erythema multiforme, hepatic function abnormal, purpura on Mar 27, 2007 from JAPAN Additional patient health information: Female patient , 64 years of age, weighting 136.7 lb, was diagnosed with hypertension, hypercholesterolaemia and. Perdipine dosage: . During the same period patient was treated with LIPITOR (Dosage Regimen Reported As 10 Mg, Uid/qd.) (View Lipitor Review and Lipitor Label ), MUCOSTA (View Mucosta Review and Mucosta Label ), TOUGHMAC E (View Toughmac E Review and Toughmac E Label ), TAKEPRON (View Takepron Review and Takepron Label ). Patient was hospitalized.

5252965-6 | Erythema Multiforme, Hepatic Function Abnormal, Purpura
Adverse event was reported on Feb 19, 2007 by a Female patient taking Perdipine (View Usage) (Dosage: ) was diagnosed with hypertension, hypercholesterolaemia and. Location: JAPAN , 64 years of age, weighting 136.7 lb, After Perdipine was administered, patient had the following side effects: erythema multiforme, hepatic function abnormal, purpura. During the same period patient was treated with LIPITOR (Dosage Regimen Reported As 10 Mg, Uid/qd.) (View Lipitor Review and Lipitor Label ), MUCOSTA (View Mucosta Review and Mucosta Label ), TOUGHMAC E (View Toughmac E Review and Toughmac E Label ), TAKEPRON (View Takepron Review and Takepron Label ). Patient was hospitalized.

5235240-5 | Cerebral Decompression, Depressed Level Of Consciousness, Headache, Hemiplegia, Intra-cerebral Aneurysm Operation, Respiratory Disorder, Subarachnoid Haemorrhage, Ventriculo-peritoneal Shunt
on Jan 30, 2007 Female patient from JAPAN , 56 years of age, was diagnosed with hypertension, hyperthyroidism, hypercholesterolaemia and was treated with Perdipine (View Usage). Patient experienced the following unwanted or unexpected effects: cerebral decompression, depressed level of consciousness, headache (What is headache?), hemiplegia, intra-cerebral aneurysm operation, respiratory disorder, subarachnoid haemorrhage, ventriculo-peritoneal shunt. Perdipine dosage: 40 Mg, Unk. During the same period patient was treated with THYRADIN S (View Thyradin S Review and Thyradin S Label ), MEVALOTIN (View Mevalotin Review and Mevalotin Label ), DIOVAN (40 Mg, Qd) (View Diovan Review and Diovan Label ). Patient was hospitalized and became disabled.

5217055-7 | Erythema Multiforme, Purpura
on Jan 15, 2007 Female patient from JAPAN , 64 years of age, was diagnosed with hypertension and was treated with Perdipine (View Usage). Patient had the following side effects: erythema multiforme, purpura. Perdipine dosage: . During the same period patient was treated with LIPITOR (View Lipitor Review and Lipitor Label ), MUCOSTA (View Mucosta Review and Mucosta Label ), TOUGHMAC E (View Toughmac E Review and Toughmac E Label ). Patient was hospitalized.

5142014-2 | Cerebral Haemorrhage, Surgery
Patient was taking Perdipine (View Usage). After Perdipine was administered, patient had the following side effects: cerebral haemorrhage, surgery (What is surgery?) on Oct 20, 2006 from JAPAN Additional patient health information: Female patient , 56 years of age, was diagnosed with hypertension, hyperthyroidism, hypercholesterolaemia and. Perdipine dosage: 40 Mg, Unk. During the same period patient was treated with THYRADIN S (View Thyradin S Review and Thyradin S Label ), MEVALOTIN (View Mevalotin Review and Mevalotin Label ), DIOVAN (40 Mg, Qd) (View Diovan Review and Diovan Label ). Patient was hospitalized.

5096181-X | Haemodialysis, Renal Impairment
Adverse event was reported on Aug 02, 2006 by a Male patient taking Perdipine (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: JAPAN , 66 years of age, Patient experienced the following unwanted or unexpected effects: haemodialysis, renal impairment. During the same period patient was treated with MICARDIS (View Micardis Review and Micardis Label ), TAKEPRON (Orodispersable Tablet) (View Takepron Review and Takepron Label ), ATELEC (View Atelec Review and Atelec Label ). Patient was hospitalized.

4971012-4 | Abdominal Pain, Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Back Pain, Bile Duct Obstruction, Bile Duct Stone, Blood Alkaline Phosphatase Increased, Blood Lactate Dehydrogenase Increased, Cholelithiasis
on Nov 14, 2005 Female patient from JAPAN , 80 years of age, was diagnosed with hypertension and was treated with Perdipine (View Usage). Patient had the following side effects: abdominal pain (What is abdominal pain?), alanine aminotransferase increased, aspartate aminotransferase increased, back pain (What is back pain?), bile duct obstruction, bile duct stone, blood alkaline phosphatase increased, blood lactate dehydrogenase increased, cholelithiasis. Perdipine dosage: 10 Mg, Bid. During the same period patient was treated with DIOVAN (20 Mg/day) (View Diovan Review and Diovan Label ), FELODIPINE (Unk, Unk) (View Felodipine Review and Felodipine Label ). Patient was hospitalized.

4950746-1 | Bile Duct Stone, Liver Disorder
on Nov 14, 2005 Female patient from JAPAN , 80 years of age, was diagnosed with hypertension and was treated with Perdipine (View Usage). After Perdipine was administered, patient had the following side effects: bile duct stone, liver disorder. Perdipine dosage: . During the same period patient was treated with DIOVAN (View Diovan Review and Diovan Label ), FELODIPINE (View Felodipine Review and Felodipine Label ). Patient was hospitalized.

4944693-9 | Abdominal Pain, Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Back Pain, Bile Duct Obstruction, Bile Duct Stone, Blood Alkaline Phosphatase Increased, Blood Lactate Dehydrogenase Increased, Cholelithiasis
Patient was taking Perdipine (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain (What is abdominal pain?), alanine aminotransferase increased, aspartate aminotransferase increased, back pain (What is back pain?), bile duct obstruction, bile duct stone, blood alkaline phosphatase increased, blood lactate dehydrogenase increased, cholelithiasis on Nov 14, 2005 from JAPAN Additional patient health information: Female patient , 80 years of age, was diagnosed with hypertension and. Perdipine dosage: 10 Mg, Bid. During the same period patient was treated with DIOVAN (20 Mg/day) (View Diovan Review and Diovan Label ), FELODIPINE (Unk, Unk) (View Felodipine Review and Felodipine Label ). Patient was hospitalized.

4910915-3 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Back Pain, Bile Duct Stone, Blood Alkaline Phosphatase Increased, Blood Lactate Dehydrogenase Increased, Blood Pressure Inadequately Controlled, Cholelithiasis, Liver Disorder
Adverse event was reported on Nov 14, 2005 by a Female patient taking Perdipine (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: JAPAN , 80 years of age, Patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, back pain (What is back pain?), bile duct stone, blood alkaline phosphatase increased, blood lactate dehydrogenase increased, blood pressure inadequately controlled, cholelithiasis, liver disorder. During the same period patient was treated with DIOVAN (View Diovan Review and Diovan Label ), FELODIPINE (View Felodipine Review and Felodipine Label ). Patient was hospitalized.

4909824-5 | Abdominal Pain, Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Back Pain, Bile Duct Obstruction, Bile Duct Stone, Blood Alkaline Phosphatase Increased, Blood Lactate Dehydrogenase Increased, Blood Pressure Inadequately Controlled
on Nov 14, 2005 Female patient from JAPAN , 80 years of age, was diagnosed with hypertension and was treated with Perdipine (View Usage). After Perdipine was administered, patient had the following side effects: abdominal pain (What is abdominal pain?), alanine aminotransferase increased, aspartate aminotransferase increased, back pain (What is back pain?), bile duct obstruction, bile duct stone, blood alkaline phosphatase increased, blood lactate dehydrogenase increased, blood pressure inadequately controlled. Perdipine dosage: 20 Mg, Bid. During the same period patient was treated with DIOVAN (20 Mg/day) (View Diovan Review and Diovan Label ), FELODIPINE (Unk, Unk) (View Felodipine Review and Felodipine Label ). Patient was hospitalized.

4892625-4 | Hyperkalaemia, White Blood Cell Count Increased
on Jun 20, 2005 Female patient from JAPAN , 69 years of age, was diagnosed with hypertension, myasthenia gravis and was treated with Perdipine (View Usage). Patient experienced the following unwanted or unexpected effects: hyperkalaemia, white blood cell count increased. Perdipine dosage: . During the same period patient was treated with PROGRAF (View Prograf Review and Prograf Label ), ALDACTONE (View Aldactone Review and Aldactone Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone 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 Perdipine 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 Perdipine quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Perdipine 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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During the same period patient was treated with ROPION, MUSCULAX, THIOPENTAL SODIUM, SEVOFLURANE, ULTIVA, DIPRIVAN, PERDIPINE, CEFAZOLIN SODIUM.

During the same period patient was treated with AMLODIPINE BESILATE (5 Mg / Day), DIOVAN (40 Mg/ Day), PERDIPINE (48 Ml), SOLU MEDROL (3000 Mg), STEROIDS NOS.

During the same period patient was treated with PERDIPINE (Unk) (View Perdipine Review and Perdipine Label ), DORMICUM (Unk) (View Dormicum Review and Dormicum Label ).

Report a Drug Side Effect. ... This anonymous Drug Side Effect Survey has 13 questions and takes less than 2 minutes to complete.

During the same period patient was treated with CONIEL, ADALAT, LASIX, PERDIPINE. Patient was hospitalized and became disabled. Cozaar Side Effects Report: 5575540-2 ...

During the same period patient was treated with PERDIPINE (View Perdipine Review and Perdipine Label ), MICARDIS (View Micardis Review and Micardis Label ), MAGNESIUM OXIDE ...

During the same period patient was treated with SEREVENT (View Serevent Review and Serevent Label ), THEO DUR (View Theo-dur Review and Theo-dur Label ), PERDIPINE (View ...

During the same period patient was treated with URSO 250 (300 Mg), ARICEPT (5 Mg), AMINOLEBAN (500 Ml), PERDIPINE (60 Mg), MONILAC (19.5 Mg), NAUZELIN (60 Mg), ARGAMATE (25 G), ...

perdipine Episodes: 4: Diagnosed with major depression.Side effects: cardiac failure, myocarditis More: phenobarbital Episodes: 4: Diagnosed with major depression ...

perdipine Episodes: 1: Diagnosed with major depression.Side effects: cardiac failure, myocarditis More: phenobarbital Episodes: 1: Diagnosed with major depression ...

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Perdipine Reactions
Abdominal PainWhat is Abdominal pain?
Alanine Aminotransferase Increased
Aspartate Aminotransferase Increased
Back PainWhat is Back pain?
Bacteraemia
Bile Duct Obstruction
Bile Duct Stone
Blood Alkaline Phosphatase Increased
Blood Lactate Dehydrogenase Increased
Blood Pressure Inadequately Controlled
Cerebral Decompression
Cerebral Haemorrhage
Cholelithiasis
Depressed Level Of Consciousness
Disseminated Intravascular Coagulation
Erythema Multiforme
Haemodialysis
HeadacheWhat is Headache?
Hemiplegia
Hepatic Function Abnormal
Hyperkalaemia
Ileus Paralytic
Inflammatory Bowel Disease
Intra-cerebral Aneurysm Operation
Liver Disorder
Papuloerythroderma Of Ofuji
Purpura
Renal Impairment
Respiratory Disorder
Stevens-johnson Syndrome
Perdipine 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 Perdipine 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!