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

DIARRHOEA ( 23 FDA reports)
PAIN ( 23 FDA reports)
ABDOMINAL PAIN ( 18 FDA reports)
NAUSEA ( 18 FDA reports)
DYSPNOEA ( 14 FDA reports)
MALAISE ( 14 FDA reports)
ABDOMINAL PAIN UPPER ( 13 FDA reports)
HEADACHE ( 13 FDA reports)
DEHYDRATION ( 11 FDA reports)
BACK PAIN ( 10 FDA reports)
CROHN'S DISEASE ( 10 FDA reports)
FALL ( 10 FDA reports)
SINUSITIS ( 10 FDA reports)
WEIGHT DECREASED ( 10 FDA reports)
CONSTIPATION ( 9 FDA reports)
DEPRESSION ( 9 FDA reports)
DIZZINESS ( 9 FDA reports)
FATIGUE ( 9 FDA reports)
HAEMORRHAGE ( 9 FDA reports)
VOMITING ( 9 FDA reports)
ALOPECIA ( 8 FDA reports)
DRUG INEFFECTIVE ( 8 FDA reports)
FLATULENCE ( 8 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 8 FDA reports)
WEIGHT INCREASED ( 8 FDA reports)
ABDOMINAL DISTENSION ( 7 FDA reports)
ANAEMIA ( 7 FDA reports)
BILIARY DYSKINESIA ( 7 FDA reports)
URINARY TRACT INFECTION ( 7 FDA reports)
ANXIETY ( 6 FDA reports)
CHEST PAIN ( 6 FDA reports)
CHOLECYSTITIS CHRONIC ( 6 FDA reports)
COLITIS ( 6 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 6 FDA reports)
DRUG DOSE OMISSION ( 6 FDA reports)
NASOPHARYNGITIS ( 6 FDA reports)
BONE PAIN ( 5 FDA reports)
BRONCHITIS ( 5 FDA reports)
DYSPEPSIA ( 5 FDA reports)
FEELING ABNORMAL ( 5 FDA reports)
FISTULA ( 5 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 5 FDA reports)
INJECTION SITE PAIN ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
OROPHARYNGEAL PAIN ( 5 FDA reports)
PAIN IN EXTREMITY ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
ABDOMINAL TENDERNESS ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
BLOOD TEST ABNORMAL ( 4 FDA reports)
CHILLS ( 4 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 4 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
DYSGEUSIA ( 4 FDA reports)
HAEMATOCHEZIA ( 4 FDA reports)
HEART RATE IRREGULAR ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 4 FDA reports)
IRRITABLE BOWEL SYNDROME ( 4 FDA reports)
LYMPH NODES SCAN ABNORMAL ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
NEOPLASM MALIGNANT ( 4 FDA reports)
OSTEOARTHRITIS ( 4 FDA reports)
PLATELET COUNT INCREASED ( 4 FDA reports)
RASH MACULAR ( 4 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
ACCIDENTAL EXPOSURE ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BIPOLAR DISORDER ( 3 FDA reports)
BLADDER DISORDER ( 3 FDA reports)
BREAST CANCER FEMALE ( 3 FDA reports)
BREAST CYST ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
COLITIS ULCERATIVE ( 3 FDA reports)
COUGH ( 3 FDA reports)
CYSTITIS INTERSTITIAL ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DYSPNOEA EXERTIONAL ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
HEPATOTOXICITY ( 3 FDA reports)
HIP ARTHROPLASTY ( 3 FDA reports)
INJECTION SITE ERYTHEMA ( 3 FDA reports)
INJECTION SITE HAEMATOMA ( 3 FDA reports)
INJURY ( 3 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 3 FDA reports)
JUGULAR VEIN THROMBOSIS ( 3 FDA reports)
LYMPHOMA ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
RESTLESS LEGS SYNDROME ( 3 FDA reports)
RHEUMATOID ARTHRITIS ( 3 FDA reports)
SEROTONIN SYNDROME ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
SUBDURAL HAEMORRHAGE ( 3 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 3 FDA reports)
TREMOR ( 3 FDA reports)
VAGINAL DISCHARGE ( 3 FDA reports)
VAGINAL INFECTION ( 3 FDA reports)
ABDOMINAL ADHESIONS ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ACUTE LEUKAEMIA ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
AORTIC ANEURYSM RUPTURE ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BLADDER OPERATION ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 2 FDA reports)
BRUXISM ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COLONIC POLYP ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
DEVICE FAILURE ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG TOLERANCE ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
ERUCTATION ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 2 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEARING IMPAIRED ( 2 FDA reports)
HIP FRACTURE ( 2 FDA reports)
HYPERCOAGULATION ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INJECTION SITE HAEMORRHAGE ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
INTESTINAL ULCER ( 2 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 2 FDA reports)
LACERATION ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 2 FDA reports)
MORPHOEA ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NEOPLASM OF APPENDIX ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
RECTAL ABSCESS ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SCLERODERMA ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SURGERY ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
VAGINITIS BACTERIAL ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
WOUND INFECTION ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADENOMYOSIS ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANTISOCIAL BEHAVIOUR ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BREAST CALCIFICATIONS ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
BURSA DISORDER ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLECYSTITIS INFECTIVE ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CRYING ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CYST ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETIC FOOT ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ENTERITIS INFECTIOUS ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FEELINGS OF WORTHLESSNESS ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC HYPOMOTILITY ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGIC CYST ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
INCISION SITE PAIN ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LABILE HYPERTENSION ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LEGIONELLA TEST POSITIVE ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NASAL DISORDER ( 1 FDA reports)
NASAL SEPTUM DEVIATION ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIODONTITIS ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 1 FDA reports)
REFLUX GASTRITIS ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 1 FDA reports)
SINUS OPERATION ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SPIDER VEIN ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPUTUM INCREASED ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
TONGUE BLISTERING ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
UTERINE ENLARGEMENT ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)

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