Please choose an event type to view the corresponding MedsFacts report:

ASTHMA ( 24 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 14 FDA reports)
PNEUMONIA ( 12 FDA reports)
PYREXIA ( 10 FDA reports)
RHABDOMYOLYSIS ( 8 FDA reports)
INTERSTITIAL LUNG DISEASE ( 7 FDA reports)
DEHYDRATION ( 6 FDA reports)
DIARRHOEA ( 6 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 6 FDA reports)
ABNORMAL BEHAVIOUR ( 5 FDA reports)
DRUG ERUPTION ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
ALOPECIA ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
CONJUNCTIVITIS ( 4 FDA reports)
DYSGEUSIA ( 4 FDA reports)
HEPATITIS ACUTE ( 4 FDA reports)
MEDIASTINITIS ( 4 FDA reports)
RASH ( 4 FDA reports)
URINARY RETENTION ( 4 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DYSURIA ( 3 FDA reports)
INCOHERENT ( 3 FDA reports)
MALAISE ( 3 FDA reports)
METASTASES TO LYMPH NODES ( 3 FDA reports)
PARONYCHIA ( 3 FDA reports)
PERSECUTORY DELUSION ( 3 FDA reports)
PROSTATE CANCER ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
WHEEZING ( 3 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BRONCHIAL WALL THICKENING ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIAC HYPERTROPHY ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DERMATITIS ACNEIFORM ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOSMIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
IMPULSIVE BEHAVIOUR ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
MUSCLE DISORDER ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NO ADVERSE EVENT ( 2 FDA reports)
OESOPHAGEAL FISTULA ( 2 FDA reports)
OESOPHAGEAL PERFORATION ( 2 FDA reports)
OTITIS MEDIA ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
PROSTATITIS ( 2 FDA reports)
PULMONARY FISTULA ( 2 FDA reports)
RESIDUAL URINE ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
VASCULAR PURPURA ( 2 FDA reports)
VOMITING ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHILLS ( 1 FDA reports)
COUGH ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EOSINOPHILIC CELLULITIS ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
IMMUNOGLOBULINS DECREASED ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
LARGE INTESTINE CARCINOMA ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 1 FDA reports)
METASTASES TO KIDNEY ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
RADIATION OESOPHAGITIS ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
THYROXINE FREE DECREASED ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 1 FDA reports)
TREMOR ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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