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Rulid Side Effects

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Common Rulid Side Effects


The most commonly reported Rulid side effects (click to view or check a box to report):

Renal Failure Acute (3)
Aspartate Aminotransferase Increased (2)
Blood Alkaline Phosphatase Increased (2)
Alanine Aminotransferase Increased (2)
Neutropenia (2)
Hepatitis (2)
Hepatic Necrosis (2)
Pharyngolaryngeal Pain (1)
Rash (1)
Pyrexia (1)
Respiratory Tract Infection (1)
Nephritis Interstitial (1)
Rhabdomyolysis (1)
Hyperhidrosis (1)
Jaundice Cholestatic (1)
Liver Function Test Abnormal (1)
Hepatitis Cholestatic (1)
Hepatic Enzyme Abnormal (1)
Haemoglobin Decreased (1)
Gamma-glutamyltransferase Increased (1)

➢ More



If you or someone in your family has experienced a serious side effect to a health product, you are encouraged to report the experience to your health care professional (e.g. physician, pharmacist). You could also complete a copy of the side effect reporting form or report your side effect to FDA.

Rulid Side Effects Reported to FDA



Rulid Side Effect Report#8271468-8
Hepatitis, Aspartate Aminotransferase Increased, Alanine Aminotransferase Increased, Hepatic Necrosis, Neutropenia
This is a report of a 31-year-old female patient (weight: NA) from France, suffering from the following health symptoms/conditions: pyrexia,breast cancer, who was treated with Rulid (dosage: 300 Mg, 1x/day, start time:
May 17, 2004), combined with:
  • Epirubicin Hydrochloride (135 Mg, Other)
  • Fluorouracil (880 Mg, Other)
  • Cyclophosphamide (880 Mg, Other)
  • Solu-medrol (Unk)
  • Zofran (8 Mg, Unk)
  • Polery Adulte (Unk)
  • Prednisolone (Unk)
  • Fluorouracil (Unk)
and developed a serious reaction and side effect(s): Hepatitis, Aspartate Aminotransferase Increased, Alanine Aminotransferase Increased, Hepatic Necrosis, Neutropenia after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Rulid treatment in female patients, resulting in Hepatitis side effect. The patient was hospitalized.
Rulid Side Effect Report#8251572-0
Hepatic Necrosis, Neutropenia, Hepatitis
This report suggests a potential Rulid Hepatic Necrosis side effect(s) that can have serious consequences. A 31-year-old female patient (weight: NA) from France was diagnosed with the following symptoms/conditions: pyrexia,breast cancer,cough and used Rulid (dosage: 150 Mg, 2x/day) starting
Apr 19, 2004. After starting Rulid the patient began experiencing various side effects, including: Hepatic Necrosis, Neutropenia, HepatitisAdditional drugs used concurrently:
  • Fluorouracil (880 Mg, Other)
  • Codeine/erysimin (Unk)
  • Fluorouracil (Unk)
  • Cyclophosphamide (Unk)
  • Zofran (8 Mg, Unk)
  • Epirubicin Hydrochloride (135 Mg, Other)
  • Desloratadine (Unk)
  • Acetaminophen (500 Mg, Unk)
The patient was hospitalized. Although Rulid demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Hepatic Necrosis, may still occur.
Rulid Side Effect Report#8139059-7
Rhabdomyolysis
This Rhabdomyolysis problem was reported by a health professional from France. A 67-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Jan 01, 2002 this consumer started treatment with Rulid (dosage: 150 Mg, Bid). The following drugs were being taken at the same time:
  • Pravastatin (40 Mg, Qd)
  • Lormetazepam (2 Mg, Qd)
  • Surmontil (100.0 Mg, Bid)
  • Pravastatin
  • Pantoprazole (40 Mg, Qd)
  • Mucomyst (200 Mg, Tid)
  • Bisoprolol Fumarate (2.5 Mg, Bid)
  • Metformin Hcl (280.0 Mg, Bid)
When using Rulid, the patient experienced the following unwanted symptoms/side effects: RhabdomyolysisThe patient was hospitalized.Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Rhabdomyolysis, may become evident only after a product is in use by the general population.
Rulid Side Effect Report#8128888-1
Eosinophilia, Eosinophilic Pneumonia
This Eosinophilia side effect was reported by a health professional from France. A 77-year-old female patient (weight:NA) experienced the following symptoms/conditions: chest x-ray abnormal.The patient was prescribed Rulid (drug dosage: 150 Mg, 2x/day), which was initiated on
Jun 01, 2005. Concurrently used drugs:
  • Previscan (Unk)
  • Mixtard Human 70/30
  • Cordarone (200 Mg, 1x/day)
  • Ramipril (Unk)
  • Oxeol (Unk)
  • Bronchodual (Unk)
  • Beclometasone (Unk)
  • Diltiazem Hcl (Unk)
.After starting to take Rulid the consumer reported adverse symptoms, such as: Eosinophilia, Eosinophilic PneumoniaThese side effects may potentially be related to Rulid. The patient was hospitalized.
Rulid Side Effect Report#8117105-4
Bronchitis, Haemoglobin Decreased, Gallbladder Disorder, Hepatitis Cholestatic, Cholelithiasis
This is a report of a 77-year-old male patient (weight: NA) from Germany, suffering from the following health symptoms/conditions: bronchitis,depression, who was treated with Rulid (dosage: 150mg, Daily, start time:
Aug 01, 2001), combined with:
  • Sertraline Hydrochloride (50 Mg, Daily)
and developed a serious reaction and side effect(s): Bronchitis, Haemoglobin Decreased, Gallbladder Disorder, Hepatitis Cholestatic, Cholelithiasis after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Rulid treatment in male patients, resulting in Bronchitis side effect. The patient was hospitalized.
Rulid Side Effect Report#7604592-0
Toxic Epidermal Necrolysis, Stevens-johnson Syndrome
This report suggests a potential Rulide Toxic Epidermal Necrolysis side effect(s) that can have serious consequences. A 45-year-old female patient (weight: NA) from Australia was diagnosed with the following symptoms/conditions: NA and used Rulide (dosage: Unk) starting NS. After starting Rulide the patient began experiencing various side effects, including: Toxic Epidermal Necrolysis, Stevens-johnson SyndromeAdditional drugs used concurrently:
  • Pristiq (Unk)
The patient was hospitalized. Although Rulide demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Toxic Epidermal Necrolysis, may still occur.
Rulid Side Effect Report#7516775-9
Renal Failure Acute, Clostridium Difficile Colitis, Sepsis, Diarrhoea, Dehydration
This Renal Failure Acute problem was reported by a pharmacist from Germany. A 90-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: tracheobronchitis. On
Dec 28, 2010 this consumer started treatment with Rulid (dosage: 300 Mg, Qd). The following drugs were being taken at the same time:
  • Unacid Pd Oral (750 Mg, Bid)
  • Humalog (14 Iu, Qd)
  • Norvasc (10 Mg, Qd)
  • Corangin ^ciba-geigy^ (40 Mg, Bid)
  • Torsemide (10 Mg, Qd)
  • Fentanyl (4.125 Mg, Q72h)
  • Pantoprazole (40 Mg, Qd)
  • Metronidazole (500 Mg, Tid)
When using Rulid, the patient experienced the following unwanted symptoms/side effects: Renal Failure Acute, Clostridium Difficile Colitis, Sepsis, Diarrhoea, DehydrationThe patient was hospitalized.Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Renal Failure Acute, may become evident only after a product is in use by the general population.
Rulid Side Effect Report#7488827-3
Cardiac Arrest, Renal Failure Acute
This Cardiac Arrest side effect was reported by a physician from Korea, Republic Of. A 39-year-old male patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Rulid (drug dosage: Unk), which was initiated on
Aug 07, 2008. Concurrently used drugs:
  • Ciprofloxacin Hydrochloride (2250 Mg Daily Dosage)
  • Teicoplanin (Unk)
  • Meropenem (Unk)
  • Ativan (Unk)
  • Lasix (Unk)
  • Voriconazole (200 Mg, 2x/day)
  • K-contin Continus (Unk)
  • Vitamin K Tab (Unk)
.After starting to take Rulid the consumer reported adverse symptoms, such as: Cardiac Arrest, Renal Failure AcuteThese side effects may potentially be related to Rulid.
Rulid Side Effect Report#7329935-7
Congenital Pyelocaliectasis, Atrial Septal Defect
This is a report of a male patient (weight: NA) from Belgium, suffering from the following health symptoms/conditions: NA, who was treated with Rulid (dosage: NA, start time: NS), combined with:
  • Maxipim
  • Viramune
  • Kaletra
  • Truvada
  • Clamoxyl
  • Rocephin
and developed a serious reaction and side effect(s): Congenital Pyelocaliectasis, Atrial Septal Defect after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Rulid treatment in male patients, resulting in Congenital Pyelocaliectasis side effect.
Rulid Side Effect Report#6657367-3
Hepatic Enzyme Abnormal
This report suggests a potential Rulid Hepatic Enzyme Abnormal side effect(s) that can have serious consequences. A 75-year-old male patient (weight: NA) from France was diagnosed with the following symptoms/conditions: NA and used Rulid (dosage: NA) starting
Apr 01, 2008. After starting Rulid the patient began experiencing various side effects, including: Hepatic Enzyme AbnormalAdditional drugs used concurrently:
  • Lasix
  • Calcium Carbonate
  • Allopurinol
  • Lexomil
  • Meteoxane
  • Myfortic
  • Hyperium
  • Zeffix
The patient was hospitalized. Although Rulid demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Hepatic Enzyme Abnormal, may still occur.
Rulid Side Effect Report#6577064-2
Alanine Aminotransferase Increased, Arthralgia, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Blood Lactate Dehydrogenase Increased, Cough, Decreased Appetite, Gamma-glutamyltransferase Increased
This Alanine Aminotransferase Increased problem was reported by a health professional from France. A 75-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Apr 01, 2008 this consumer started treatment with Rulid (dosage: NA). The following drugs were being taken at the same time:
  • Lasix
  • Eucalcic
  • Allopurinol
  • Lexomil
  • Meteoxane
  • Myfortic
  • Hyperium
  • Zeffix
When using Rulid, the patient experienced the following unwanted symptoms/side effects: Alanine Aminotransferase Increased, Arthralgia, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Blood Lactate Dehydrogenase Increased, Cough, Decreased Appetite, Gamma-glutamyltransferase IncreasedThe patient was hospitalized.Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Alanine Aminotransferase Increased, may become evident only after a product is in use by the general population.
Rulid Side Effect Report#5074918-3
Abdominal Tenderness, Blood Alkaline Phosphatase Increased, Hyperhidrosis, Jaundice Cholestatic, Liver Function Test Abnormal, Pharyngolaryngeal Pain, Pyrexia, Rash, Respiratory Tract Infection
This Abdominal Tenderness side effect was reported by a physician from Australia. A 30-year-old female patient (weight:NA) experienced the following symptoms/conditions: respiratory tract infection,schizophrenia, paranoid type.The patient was prescribed Rulide (drug dosage: NA), which was initiated on
Sep 11, 1997. Concurrently used drugs:
  • Clozaril (25 - 125 Mg Daily)
  • Clozaril (75 - 300mg Daily)
  • Sertraline (50 Mg)
  • Flupentixol (Depot)
  • Clonazepam (0.5 Mg, Qd)
.After starting to take Rulide the consumer reported adverse symptoms, such as: Abdominal Tenderness, Blood Alkaline Phosphatase Increased, Hyperhidrosis, Jaundice Cholestatic, Liver Function Test Abnormal, Pharyngolaryngeal Pain, Pyrexia, Rash, Respiratory Tract InfectionThese side effects may potentially be related to Rulide.
Rulid Side Effect Report#5029689-3
Nephritis Interstitial, Renal Failure Acute
This is a report of a 37-year-old female patient (weight: NA) from , suffering from the following health symptoms/conditions: gastroenteritis,nasopharyngitis, who was treated with Rulid (dosage: NA, start time:
Apr 05, 2006), combined with: NA. and developed a serious reaction and side effect(s): Nephritis Interstitial, Renal Failure Acute after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Rulid treatment in female patients, resulting in Nephritis Interstitial side effect. The patient was hospitalized.



The appearance of Rulid on this list does not mean that FDA has concluded that the drug has the listed risk. It means that FDA has identified a potential safety issue, but it does not mean that FDA has found a causal relationship between the drug and the listed risk.

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Track Your Side Effects

Note Your Observations

It is really important to keep track of your health symptoms, right from the time you start a new medicine. You can do it any way you prefer: in a notebook, in a computer file or using our online tool. You should also note down any other medicines you are taking at the same time, because there could be an interaction between these medicines.

Why Your Notes are Important

Your notes could be helpful in several ways:

  • You can use them to remind you of details that may alert your health care professional(s) to a problem
  • You will have a record to refer to in the future, in case you are ever prescribed the same medicine again

  • Log Form

    You can use the following log form to write down important information, like the date and time you experienced a side effect and your symptoms, how strong the symptoms were, and any other medicines you were using.

    Medicine Name and Dosage:
    Side Effects Scale Date & Time Other Medicine(s) or Treatment(s)
    Scale: 1 = very mild to 10 = very bad

    Side effects reports are analyzed to discover potential health product safety signals. Some important reactions may take an extremely long time to develop or occur infrequently. Continued monitoring of adverse reactions is thus essential to maintain a comprehensive safety and effectiveness profile of health products.

    You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.

    Rulid reports list potential signals of serious risks and new safety information that were identified using the FDA Adverse Event Reporting System (FAERS).
    FAERS is a database that contains information on adverse event and medication errors reports submitted to FDA by healthcare professionals (such as physicians, pharmacists, nurses and others), consumers (such as patients, family members, layers and others) and manufacturers.

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    Rulid Safety Alerts, Active Ingredients, Usage Information

    More About Rulid

    Side Effects reported to FDA: 13

    Rulid safety alerts: No

    Reported deaths: 2

    Reported hospitalizations: 9

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