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

DYSPNOEA ( 16 FDA reports)
FATIGUE ( 14 FDA reports)
HYPERSENSITIVITY ( 12 FDA reports)
PNEUMONIA ( 12 FDA reports)
CHEST DISCOMFORT ( 11 FDA reports)
HEADACHE ( 11 FDA reports)
URTICARIA ( 11 FDA reports)
VOMITING ( 11 FDA reports)
ARTHRALGIA ( 10 FDA reports)
CONDITION AGGRAVATED ( 10 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 9 FDA reports)
DEHYDRATION ( 9 FDA reports)
ANAEMIA ( 8 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 8 FDA reports)
ASTHENIA ( 8 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 8 FDA reports)
DRUG INEFFECTIVE ( 8 FDA reports)
NAUSEA ( 8 FDA reports)
OEDEMA PERIPHERAL ( 8 FDA reports)
PAIN ( 8 FDA reports)
PAIN IN EXTREMITY ( 8 FDA reports)
WEIGHT DECREASED ( 8 FDA reports)
WHEEZING ( 8 FDA reports)
ASTHMA ( 7 FDA reports)
DIARRHOEA ( 7 FDA reports)
DIZZINESS ( 7 FDA reports)
MYALGIA ( 7 FDA reports)
PRURITUS ( 7 FDA reports)
ANAPHYLACTIC REACTION ( 6 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 6 FDA reports)
CELLULITIS ( 6 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 6 FDA reports)
HYPERHIDROSIS ( 6 FDA reports)
MULTIPLE SCLEROSIS ( 6 FDA reports)
PLEURAL EFFUSION ( 6 FDA reports)
PYREXIA ( 6 FDA reports)
RENAL FAILURE ( 6 FDA reports)
BLOOD BILIRUBIN INCREASED ( 5 FDA reports)
BLOOD GLUCOSE INCREASED ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
CHOLELITHIASIS ( 5 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 5 FDA reports)
COUGH ( 5 FDA reports)
FLUSHING ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
PALPITATIONS ( 5 FDA reports)
PREGNANCY ( 5 FDA reports)
SINUSITIS ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 4 FDA reports)
ALOPECIA ( 4 FDA reports)
ARTHROPOD BITE ( 4 FDA reports)
ATELECTASIS ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
CHILLS ( 4 FDA reports)
DIASTOLIC DYSFUNCTION ( 4 FDA reports)
DRUG TOXICITY ( 4 FDA reports)
DYSPHONIA ( 4 FDA reports)
FALL ( 4 FDA reports)
IMPAIRED WORK ABILITY ( 4 FDA reports)
INFLUENZA LIKE ILLNESS ( 4 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 4 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 4 FDA reports)
METASTATIC NEOPLASM ( 4 FDA reports)
MIGRAINE ( 4 FDA reports)
MOUTH ULCERATION ( 4 FDA reports)
RASH ( 4 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 4 FDA reports)
SWELLING FACE ( 4 FDA reports)
SWOLLEN TONGUE ( 4 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 3 FDA reports)
AMENORRHOEA ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
BLOOD PROLACTIN INCREASED ( 3 FDA reports)
BRAIN OEDEMA ( 3 FDA reports)
BREAST CYST ( 3 FDA reports)
BREAST FIBROSIS ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
DEATH ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DRUG DOSE OMISSION ( 3 FDA reports)
EAR PAIN ( 3 FDA reports)
EOSINOPHIL COUNT INCREASED ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
GALLBLADDER DISORDER ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
HOT FLUSH ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
OSTEONECROSIS ( 3 FDA reports)
PAIN IN JAW ( 3 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PERITONEAL HAEMORRHAGE ( 3 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 3 FDA reports)
PNEUMONIA VIRAL ( 3 FDA reports)
POST PROCEDURAL PAIN ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
PULMONARY HYPERTENSION ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ABORTION ( 2 FDA reports)
ABSCESS JAW ( 2 FDA reports)
ACUTE PRERENAL FAILURE ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
AUTOIMMUNE DISORDER ( 2 FDA reports)
BILIARY DILATATION ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BREAST CANCER FEMALE ( 2 FDA reports)
BREAST CANCER IN SITU ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
COMA ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DIAPHRAGMATIC DISORDER ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FIBROADENOMA OF BREAST ( 2 FDA reports)
FISTULA ( 2 FDA reports)
FOOD POISONING ( 2 FDA reports)
GALLBLADDER POLYP ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
INTENTIONAL MISUSE ( 2 FDA reports)
INTRA-UTERINE DEATH ( 2 FDA reports)
LACRIMATION INCREASED ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LIBIDO DECREASED ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MENINGITIS MENINGOCOCCAL ( 2 FDA reports)
METASTASES TO LUNG ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
MUSCLE CRAMP ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
OSTEITIS ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PACEMAKER COMPLICATION ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PATHOLOGICAL FRACTURE ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PLEURITIC PAIN ( 2 FDA reports)
POLYMYOSITIS ( 2 FDA reports)
PORTAL VEIN THROMBOSIS ( 2 FDA reports)
POST PROCEDURAL INFECTION ( 2 FDA reports)
POSTNASAL DRIP ( 2 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RADIATION PNEUMONITIS ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
RHEUMATOID FACTOR INCREASED ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SERUM SICKNESS ( 2 FDA reports)
SNEEZING ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TOOTH ABSCESS ( 2 FDA reports)
TORSADE DE POINTES ( 2 FDA reports)
TRIGEMINAL NEURALGIA ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL AORTIC BRUIT ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADRENAL MASS ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 1 FDA reports)
ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BENIGN BREAST NEOPLASM ( 1 FDA reports)
BICYTOPENIA ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST CANCER STAGE II ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CARCINOMA ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
COITAL BLEEDING ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COMPLEMENT FACTOR C1 INCREASED ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CRYING ( 1 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DENTAL DISCOMFORT ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FISTULA DISCHARGE ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 1 FDA reports)
GASTRIC OUTLET OBSTRUCTION ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GINGIVAL RECESSION ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HILAR LYMPHADENOPATHY ( 1 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOTRICHOSIS ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INNER EAR INFLAMMATION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
JOINT LOCK ( 1 FDA reports)
JOINT SPRAIN ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG CREPITATION ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOUTH PLAQUE ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
NASAL MUCOSA ATROPHY ( 1 FDA reports)
NASAL POLYPS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE I ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
ORAL INFECTION ( 1 FDA reports)
ORAL MUCOSA ATROPHY ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
OVULATION PAIN ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE ABNORMAL ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERICARDITIS LUPUS ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POSTOPERATIVE THROMBOSIS ( 1 FDA reports)
PREGNANCY TEST POSITIVE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATE CANCER RECURRENT ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RECTAL FISSURE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SWELLING ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TWIN PREGNANCY ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
UTERINE PERFORATION ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WEGENER'S GRANULOMATOSIS ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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