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

MYALGIA ( 9 FDA reports)
ASTHMA ( 8 FDA reports)
CONTUSION ( 8 FDA reports)
ARTHRALGIA ( 7 FDA reports)
CONDITION AGGRAVATED ( 7 FDA reports)
URTICARIA ( 7 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 6 FDA reports)
ABDOMINAL PAIN LOWER ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
PAIN IN EXTREMITY ( 5 FDA reports)
PALPITATIONS ( 5 FDA reports)
WHEEZING ( 5 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
NEUROPATHY PERIPHERAL ( 4 FDA reports)
PERICARDIAL EFFUSION ( 4 FDA reports)
PLATELET COUNT INCREASED ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
CIRCULATORY COLLAPSE ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
ENCEPHALITIS ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
MYOPERICARDITIS ( 3 FDA reports)
PREGNANCY ( 3 FDA reports)
PSEUDOMONAS INFECTION ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
ABSCESS INTESTINAL ( 2 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DIVERTICULUM ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FACTOR VIII INHIBITION ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HEPATIC CYST ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INJECTION SITE MASS ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
MONONEUROPATHY MULTIPLEX ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
MYOPATHY STEROID ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RASH ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
UTERINE SPASM ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BENIGN BREAST NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CLUBBING ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COMA ( 1 FDA reports)
CYSTIC FIBROSIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIAPHRAGM MUSCLE WEAKNESS ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INGUINAL MASS ( 1 FDA reports)
INJECTION SITE BURNING ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MASS ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PAIN ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURAL RUB ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POST PROCEDURAL NAUSEA ( 1 FDA reports)
POST PROCEDURAL VOMITING ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
RADIATION PNEUMONITIS ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL SCAN ABNORMAL ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RETROPERITONEAL NEOPLASM ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SCAR ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SLIPPED FEMORAL EPIPHYSIS ( 1 FDA reports)
SMALL INTESTINAL PERFORATION ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
TENDINOUS CONTRACTURE ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VITILIGO ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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